Selected Hereditary Diseases




Approach to the child with a genetic skin condition


To effectively care for an affected newborn and provide information for anxious parents, an organized diagnostic approach is essential. The physical exam requires special attention to ectodermal involvement by assessing the hair, teeth, nails, palms and soles of the feet. Moving beyond the skin, a child should be examined for dysmorphic features, associated major or minor congenital anomalies and accompanying illness. Results of a newborn hearing screen and pediatric ophthalmology exam are often valuable. Finally, a detailed family history including ethnic background and miscarriage history is beneficial. After gathering clinical information, superb resources are available online to consider diagnostic possibilities. One example is Online Mendelian Inheritance in Man (OMIM; www-ncbi-nlm-nih-gov.easyaccess1.lib.cuhk.edu.hk/omim ).


OMIM is maintained by the National Center for Biotechnology Information (NCBI) and can be searched using a list of the clinical features in an affected patient. Each disorder is assigned a number based on broad categories such as inheritance pattern. ‘GeneTests’ ( www-ncbi-nlm-nih-gov.easyaccess1.lib.cuhk.edu.hk/sites/GeneTests ) and a separate database, ‘GeneReviews’ offers a frequently updated list of internationally available DNA-based genetic tests and concise, yet comprehensive overviews of selected disorders. For effective coordination of testing and advising the patient about the complexities of genetic testing and reproductive options, the GeneTests site provides a database of genetics services that is searchable by country and province or state. Increasingly, individual mutations that cause familial genetic disorders are recognized to affect important regulatory pathways. This chapter highlights pathways that are particularly important to growth and development of the skin.




Disorders of the RAS-MAPK pathway (RASopathies)


Several genetic skin disorders are caused by mutations in genes in the RAS-MAPK signaling pathway ( Fig. 29.1 ) and have been coined the ‘RASopathies’. The RASopathies include neurofibromatosis-1 (NF-1), NF-like syndrome (Legius syndrome), Noonan syndrome, Noonan with multiple lentigines (formerly LEOPARD syndrome), cardiofaciocutaneous syndrome, Costello syndrome, capillary malformation–arteriovenous malformation (see Chapter 22 ), and hereditary gingival fibromatosis ( Table 29.1 ). Neurofibromatosis and Legius syndrome are also discussed in Chapter 24 .




Figure 29.1


The RAS/mitogen-activated protein kinase (MAPK) signaling pathway is important in cell proliferation, differentiation, motility, apoptosis and senescence.

Disorders resulting from mutations in the genes of the RAS/MAPK have been coined the RASopathies and include Noonan, multiple lentigines syndrome, gingival fibromatosis 1, neurofibromatosis 1, capillary malformation-arteriovenous malformation, Costello, autoimmune lymphoproliferative (ALPS), cardiofaciocutaneous and Legius syndromes.

(Adapted from Curr Opin Genet Dev 2009; 19(3):230–236. Published online 2009 May 19. doi: 10.1016/j.gde.2009.04.001.)


TABLE 29.1

Comparison of the clinical features of the RASopathies




















































NF-1 Cardiofacio-cutaneous syndrome Costello syndrome Noonan syndrome Multiple lentigines syndrome Capillary malformation- arteriovenous malformation
Gene NF1 BRAF, MEK1, MEK2, KRAS HRAS PTPN11, SOS1, KRAS, NRAS, RAF1, SHOC2, CBL and BRAF PTPN11, RAF, BRAF RASA1
Dermatologic features Café-au-lait macules
Intertriginous freckling
Neurofibromas
Plexiform neurofibroma
Ulerythema ophryogenes
Keratosis pilaris
Melanocytic nevi
Infantile hemangiomas
Papillomata of the nose and perianal region
Palmoplantar hyperkeratosis
Redundant skin on the hands and feet
Acanthosis nigricans
Congenital lymphedema
Café-au-lait macules
Keratosis pilaris (most common with SOS1 mutations)
Lentigines
Café noir patches
Capillary malformations
Arteriovenous malformations of the brain, spine, skin, muscle and bone
Cardiac features Uncommon Pulmonic stenosis
Hypertrophic cardiomyopathy
Pulmonic stenosis
Hypertrophic cardiomyopathy
Pulmonic stenosis
Hypertrophic cardiomyopathy
EKG abnormalities
Pulmonic stenosis
Hypertrophic cardiomyopathy
Rare
Tumor predisposition Yes:
Optic glioma
Hematologic malignancies
Meningioma and other brain cancers
Malignant peripheral nerve sheath tumor
Pheochromocytoma
Rare:
Possible risk for ALL and lymphoma
Yes:
Malignant solid tumors
(rhabdomyosarcoma, neuroblastoma, transitional cell carcinoma of the bladder)
Rare:
Hematologic malignancies
Rare:
Hematologic malignancies
Rare:
Possible increased risk for neural tumors
Other Lisch nodules
Learning disability
Pseudoarthrosis
Macrocephaly
Sphenoid wing dysplasia
Renal artery stenosis
Hypertension
Failure to thrive (severe)
Developmental delay
Failure to thrive (mild)
Developmental delay
Sociable, outgoing personality
Low posterior hairline
Webbed neck
Pectus excavatum
Bleeding tendency
Short stature
Ocular hypertelorism
Sensorineural hearing loss
Short stature
Risk for intracranial and spinal arteriovenous malformation
Parkes–Weber syndrome


Neurofibromatosis type 1


Neurofibromatosis 1 (NF-1, MIM #162200) is a multisystem disorder characterized by age-related abnormalities of tissue proliferation. NF-1 is one of the most common autosomal dominant genetic conditions with an incidence of approximately 1 in 3000 individuals. Consensus criteria for the diagnosis of NF-1 were established at the 1988 NIH conference to be used as a guideline for clinical diagnosis ( Box 29.1 ). In 95% of affected individuals, a diagnosis can be made by age 11 through the use of clinical evaluation alone. However, NF-1 can be a difficult condition to diagnose in some infants due to the high incidence of sporadic mutations, variability of clinical expression, and age-related penetrance of individual clinical manifestations. Hence, anticipatory guidance counseling should be provided in both established and suspected cases of NF-1.



Box 29.1

NIH consensus criteria for neurofibromatosis 1





  • ≥6 café-au-lait macules >5 mm in greatest diameter in prepubertal individuals or >15 mm in greatest diameter after puberty



  • ≥2 neurofibromas of any type, or ≥1 plexiform neurofibromas



  • Axillary/inguinal freckling (Crowe’s sign)



  • Tumor of the optic nerve pathway (optic glioma)



  • ≥2 Lisch nodules (iris hamartomas)



  • Distinctive osseous changes (e.g., sphenoid wing dysplasia or pseudoarthrosis)



  • First-degree relative with NF-1




Cutaneous findings


Café-au-lait macules (CALM) are light to dark brown sharply defined oval macules and patches which can occur on almost any skin surface ( Fig. 29.2A ). Infants with ≥6 café-au-lait macules >5 mm in diameter that are not confined to a single segmental region, should be evaluated and managed as though they have NF-1, even without other signs of NF-1, because of the high likelihood that they will develop other diagnostic signs with time. At puberty, if other features are lacking, the approach and diagnosis can be reconsidered.




Figure 29.2


(A) Multiple café-au-lait macules in an infant with neurofibromatosis. (B) Axillary freckling and multiple café-au-lait macules. (C) Plexiform neurofibroma of the hip of a 2-year old boy. Note the ill-defined borders and dark brown color in comparison to the sharp borders and light brown color of the café-au-lait macule on the thigh.

(Courtesy of Dr V.P. Sybert.)






Intertriginous freckling of the axillary and inguinal regions may occasionally be present in infancy, but most often present between 2–10 years of age ( Fig. 29.2B ). Although freckling on the neck and trunk is common in NF-1, it is not accepted as a diagnostic criterion.


Peripheral neurofibromas are infrequent in early childhood NF-1, occurring in only 14% of children less than 10 years of age. Often the first sign of dermal neurofibromas are 3–6 mm, light blue, minimally raised papules which are most easily detected with side lighting. It has been suggested that a subset of children with large deletions of the NF-1 gene typically present with multiple neurofibromas in early childhood.


Plexiform neurofibromas may be apparent at birth or soon thereafter; however because they are often internal, may be difficult to detect. They occur in at least 25% of affected individuals ( Fig. 29.2C ). Most have overlying hyperpigmentation; some – but not all – have increased vascularity resembling a vascular anomaly or hypertrichosis resembling a congenital melanocytic nevus. Plexiform neurofibromas may grow rapidly and interdigitate with and surround normal structures. Radiologic imaging and neurosurgical consultation should be considered if lesions are extensive or close to major nerve bundles.


Extracutaneous findings


Optic gliomas are astrocytomas arising anywhere along the optic pathway. These lesions tend to arise in infancy or early childhood. Half of the tumors are symptomatic, causing loss of visual acuity, decreased field of vision, proptosis, or interference with the hypothalamopituitary axis. Symptomatic optic gliomas are often diagnosed by 6 years of age.


Lisch nodules are pigmented iris hamartomas that rarely present in infants, and only 20% of individuals under 5 years of age with NF-1 have Lisch nodules. They are best seen on slit-lamp examination and do not result in functional disability. Congenital glaucoma occurs in less than 0.05% of individuals with NF-1 and may present with an ipsilateral neurofibroma of the eyelid.


Relatively short stature and large head size are frequent findings and more common than the more diagnostic skeletal changes, pseudoarthrosis and sphenoid wing dysplasia. Pseudoarthrosis represents the failure of union after fracture. It is always unilateral and most commonly presents in the tibia as anterolateral bowing. Ultimately, pseudoarthrosis can progress to severe deformity. Sphenoid wing dysplasia is a unilateral defect of the orbit present in approximately 5% of individuals with NF-1 and results in a change in orbit structure. Approximately half of those cases with sphenoid wing dysplasia develop an ipsilateral temporal–orbital plexiform neurofibroma, and half of individuals presenting with a temporal–orbital tumor also have an underlying plexiform neurofibroma. Learning disabilities occur in approximately 50% of children with NF-1. The main learning difficulties include reading, deficits in perceptual skills (visuospatial) and executive functioning. Attention issues are also common.


Etiology and pathogenesis


NF-1 is due to an autosomal dominant mutation localized to chromosome 17 that results in defects in neurofibromin, a tumor suppressor protein that stimulates hydrolysis of guanosine triphosphate (GTP) bound to ras .


Differential diagnosis and diagnosis


Café-au-lait macules may be found in many other conditions, including segmental pigmentary disorder and McCune–Albright syndrome (see Chapter 24 ). Additional differential diagnoses for multiple café-au-lait macules are shown in Box 29.2 . Genetic testing for NF-1 is available from several commercial and research laboratories (see: www.genetests.org , for specific information). Decisions regarding whether laboratory-based NF testing is appropriate are best made in conjunction with a geneticist and genetic counselor.



Box 29.2

Differential diagnosis for multiple café-au-lait macules





  • Legius syndrome



  • Neurofibromatosis type 2



  • Schwannomatosis



  • Noonan syndrome



  • Noonan syndrome with multiple lentigines (LEOPARD syndrome)



  • Multiple endocrine neoplasia 2B



  • Bannayan–Riley–Ruvalcaba syndrome



  • Piebald trait




Treatment and care


Patients with neurofibromatosis require age-related anticipatory guidance counseling and regular follow-up with a pediatrician, ophthalmologist and geneticist. Additional specialists can be included, based on symptoms or complications and may include orthopedics, neurology, dermatology, neuropsychology, and neurosurgery ( Box 29.3 ). Ophthalmologists and neurologists should evaluate for optic nerve pathway tumors and glaucoma. Anterolateral tibial bowing when present require prompt orthopedic evaluation, because the critical time for fracture and poor healing is infancy to early childhood. Periodic evaluation for scoliosis is also necessary. Regular physical examinations should include careful measurement of blood pressure because of a higher incidence of hypertension secondary to renovascular disease, vasoactive secreting tumors, and coarctation of the aorta. Head circumference should be monitored because of the risk of hydrocephalus and the occurrence of macrocephaly without hydrocephalus. Careful developmental assessment is a key part of management, as the risk of neurologic abnormalities and learning disabilities is increased.



Box 29.3

Care plan

Extracutaneous manifestations of neurofibromatosis 1





  • Routine history and physical examination by a pediatrician



  • Yearly blood pressure monitoring



  • Baseline and annual ophthalmologic examination



  • Routine neurologic and developmental evaluation



  • Regular head circumference monitoring



  • Genetic counseling with discussion of genetic testing



  • Imaging based on neurologic signs and symptoms




Dermal neurofibromas are benign and should only be excised if they are symptomatic or disfiguring. Plexiform neurofibromas require close evaluation. Skin should be palpated carefully as plexiform neurofibromas may remain below the surface. If there are symptoms or neurologic abnormalities on clinical exam, MRI scans should be obtained to determine the extent of plexiform neurofibromas. Serial imaging or volumetric MRI may be necessary to assess potential growth. Pain and/or growth may herald malignant transformation, but this is exceedingly rare in infancy. Neurologic compromise may result from perineural extension, however, and neurology and/or neurosurgery may need to be consulted for plexiform lesions near neurovascular structures (such as the neck, axilla and spinal area). Orbitotemporal neurofibromas may be better managed by numerous surgical procedures over time; plastic surgery should be involved early for management of these tumors.


Leguis syndrome


Legius syndrome (MIM #611431) was first recognized in 2007 as an NF-1-like syndrome in families with multiple café-au-lait macules, but negative NF-1 gene testing. The phenotype is milder than NF-1 and seems to lack the propensity for tumor development. The clinical features include a mild NF-like phenotype and 50% of these patients meet diagnostic criteria for NF-1. Of the diagnostic criteria for NF-1 ( Box 29.1 ), the features that have been reported in Legius include >6 CALM >5 mm, intertriginous freckling, positive family history, macrocephaly, short stature and learning disabilities. Neurofibromas, plexiform neurofibromas, bone dysplasia and scoliosis have not been associated with Legius syndrome. Legius syndrome is caused by loss of function (LOF) mutations in the SPRED1 gene. Like neurofibromin, SPRED1 is a negative regulator of the RAS-MAPK pathway ( Fig. 29.1 ).


Noonan syndrome


Noonan syndrome (MIM #163950) is an autosomal dominant multisystem disorder characterized by congenital lymphedema, broad or webbed neck, low posterior hairline, short stature, and cardiac malformations ( Box 29.4 ).



Box 29.4

Clinical features

Noonan syndrome


Dermatologic associations





  • Webbed neck



  • Cutis vertices gyrata



  • Ulerythema ophryogenes



  • Koilonychia



  • Thick, curly and wooly hair



  • Prominent fetal finger pads



Extracutaneous manifestations





  • Short stature



  • Craniofacial:




    • Ptosis



    • Downslanting palpebral fissures



    • High palate




  • Cardiac pulmonic stenosis



  • Cryptorchidism




Cutaneous findings


The neonate with Noonan syndrome is unlikely to have skin manifestations other than nuchal webbing and peripheral lymphedema that suggest the diagnosis. Keratosis pilaris atrophicans faciei (ulerythema ophryogenes), characterized by horny, whitish, hemispherical, or acuminate papules at the opening of pilosebaceous follicles, is generally noted in older children, but may manifest in the external third of the eyebrows by a few months after birth. Some children with Noonan syndrome have multiple CALM and/or lentigines.


Extracutaneous findings


Neonates have a characteristic facial appearance consisting of a tall forehead, low posterior hairline, hypertelorism, down­slanting palpebral fissures, epicanthal folds, short and broad, depressed nasal root, deeply grooved philtrum and microg­nathia. The chest shape is unique with superior pectus carinatum and inferior pectus excavatum. Feeding difficulties, gastroesophageal reflux and failure to thrive are frequent problems in infancy. Unilateral or bilateral cryptorchidism are common in boys. Infants are at risk for transient monocytosis, thrombocytopenia and myeloproliferative disorder. Coagulation defects occur in approximately one-third of patients with Noonan syndrome and may present with easy bruising or prolonged bleeding times. There is a slightly increased risk of hematologic malignancy (most commonly juvenile myelomonocytic leukemia, JMML) compared with the general population. The classic congenital heart defect in Noonan syndrome is pulmonic stenosis.


Etiology and pathogenesis


The incidence of Noonan syndrome is approximately 1 in 1000–2500 live births. Noonan syndrome may be caused by a mutation in one of several genes in the RAS-MAPK signaling pathway, including PTPN11 , SOS1 , KRAS , NRAS , RAF1 , SHOC2 , CBL, and BRAF . PTPN11 and CBL mutations have a higher rate of bleeding diathesis and JMML. Patients with SOS1 mutations have a lower rate of intellectual disability. SHOC2 mutations have been associated with a Noonan phenotype with loose anagen hair. PTPN11 mutations are also the genetic basis of Noonan with multiple lentigines (formerly known as LEOPARD syndrome; see Chapter 24 ).


Differential diagnosis


In the neonatal period, the RASopathies can be very difficult to distinguish as they share the features of congenital heart defects, severe feeding difficulties and developmental delay. Later in infancy, facial and ectodermal features become more distinct for each of the RASopathies. Cardiofaciocutaneous syndrome and Costello syndrome are described in more detail below.


Treatment and care


Patients with Noonan syndrome should be monitored for growth deficiency and developmental delay. Electrocardiogram and echocardiography should be performed at the time of diagnosis and repeated as indicated based on findings. A renal ultrasound is recommended at diagnosis. Coagulopathy work-up should be performed if the patient has a history of either easy bruising or prolonged bleeding.


Cardiofaciocutaneous syndrome


Cardiofaciocutaneous (CFC) syndrome (MIM #115150) is characterized by short stature, congenital heart defects, intellectual disability, ectodermal abnormalities and a characteristic coarse facial appearance ( Table 29.2 ). Numerous cutaneous findings have been reported in CFC. In 2010, Siegel and colleagues evaluated the cutaneous manifestations in 61 mutation-positive individuals with CFC syndrome. All had dermatologic findings. One of the striking features identified in this study was a high number of melanocytic nevi. In the study, 23% of participants had over 50 nevi and 36% of those patients reported over 100 nevi. The amount of nevi increased with age and were not a prominent feature in infancy. Keratosis pilaris and ulerythema ophryogenes were very common and affected the majority of individuals in childhood and adolescence ( Fig. 29.3 ). Infantile hemangiomas occurred at a greater frequency when compared with the general population. Additional features in CFC include macrocephaly, characteristic facial appearance, growth retardation, cardiac defects, neurologic impairment, gastrointestinal dysfunction, and ocular abnormalities.



TABLE29.2

Dermatologic features found in cardiofaciocutaneous syndrome compared with Costello syndrome

(Adapted from Siegel DH, Mann JA, Krol AL, Rauen KA. Dermatological phenotype in Costello syndrome: consequences of Ras dysregulation in development. Br J Dermatol 2012; 166(3):601–607.)






































Percentage of cases
Cardiofaciocutaneous Costello
Curly hair 93.4% 95.7%
Eyebrow density 90.0% sparse 47.8% thick
Keratosis pilaris 80.3% 32.6%
Infantile hemangioma 26.2% 10.9%
Papillomas 4.9% 71.7%
More than 50 nevi 23.0% 4.0%
Palmoplantar keratoderma 36.1% 76.1%



Figure 29.3


Cardiofaciocutaneous syndrome in an infant with a confirmed BRAF mutation. The sparse curly hair and eyebrows and characteristic facial features are evident.

(Courtesy of Brenda Conger, CFC International.)


CFC syndrome is caused by mutations in BRAF , MEK1 or MEK2 . These mutations were discovered in part because of the similarity of the phenotypic features of Noonan and Costello syndromes, both of which were known to have mutations involving the RAS-MAPK pathway. Given insights into genetics and pathogenesis, it is not surprising that the main differential diagnoses for CFC syndrome include Noonan and Costello syndromes.


Costello syndrome


Costello syndrome (CS) (MIM #218040) is a rare, autosomal dominant, multiple congenital anomaly syndrome associated with failure to thrive, developmental delay, and an increased risk of malignancy. The features of Costello syndrome in the neonatal and infantile period include macrosomia, severe feeding problems, developmental delay, coarse facial features, gingival hyperplasia, osteopenia, hypertrophic cardiomyopathy and atrial arrhythmias. The most common malignancies include rhabdomyosarcoma, neuroblastoma and transitional cell cancer of the bladder. CS is caused by mutations in the HRAS gene, at 11p15.5, leading to constitutive activation of the RAS-MAPK pathway. The cutaneous findings include curly hair, papillomas on the perinasal, perioral and perianal skin, palmoplantar keratoderma, unusual body odor and heat intolerance. The skin on hands is loose and redundant ( Fig. 29.4A ). Acanthosis nigricans has been reported in 37% of the cases ( Fig. 29.4B ). In the neonatal period, it can be difficult to distinguish Costello, CFC and Noonan syndromes, as all three conditions can manifest with neonatal macrosomia, coarse facial features, failure to thrive and developmental delay.




Figure 29.4


(A) The characteristic loose, redundant skin of the hand and (B) acanthosis nigricans behind the ear lobe in an individual with Costello syndrome.




Capillary malformation-arteriovenous malformation (CM-AVM) (MIM #608354)


CM-AVM is an autosomal dominant disorder characterized by multiple, small, oval capillary malformations on the face, body and limbs, which are associated with arteriovenous malformations in about 30% of cases. The AVMs can occur in the brain, spine, muscle or skin. CM-AVM is caused by mutations in the RASA1 gene. See Chapter 22 for a more in-depth discussion about this condition.


Neurofibromatosis type 2


Neurofibromatosis type 2 (NF-2) (MIM #101000) is an autosomal dominant condition characterized by a high burden of schwannoma and meningioma tumor development.


Presentation in infancy is rare, although cutaneous schwannomas have been reported. Cutaneous features which may be present in infancy or early childhood include CALM and cutaneous schwannomas ( Fig. 29.5 ). The age range at the onset of NF-2-related symptoms is 5–55 years. The initial symptoms that lead to the diagnosis include hearing loss, visual disturbance, and enlarging subcutaneous mass. The incidence of NF-2 is difficult to predict due to a high rate of mosaicism, but is estimated at about 1 : 25 000. NF-2 is caused by mutations in the merlin (also called schwannomin) tumor suppressor gene on chromosome 22q12. The differential diagnosis for NF-2 includes NF-1 and schwannomatosis.




Figure 29.5


Cutaneous schwannomas presenting as multilobulated, pink to flesh colored rubbery plaques in an infant.

(Courtesy of Dr S. Galbraith.)




Disorders of the PI3K-AKT/mTOR pathway and overgrowth syndromes


Overgrowth syndromes and human cancer share disruption of similar critical regulatory pathways ( Table 29.3 ). Intensive cancer research, therefore, has improved our understanding of these rare but important disorders. The phosphatidylinositol 3-kinase (PI3K)-AKT pathway, in particular, critically guides cell growth and metabolism ( Fig. 29.6 ). The PI3K enzymes are a family of highly conserved enzymes that regulate cell growth, migration and survival and disruption in the embryonic period typically impacts vascular, limb or brain development. Mutations cause recognizable patterns of increased cell number, hypertrophy, increased interstitium, or a combination of these. Typical neonatal clues of an overgrowth syndrome are abnormally increased body length, macrosomia, and macrocephaly, dysregulated growth of a body part or asymmetry ( Fig. 29.7 ). Almost all overgrowth syndromes are associated with neoplasms, especially solid tumors.



TABLE 29.3

Overgrowth syndromes and associated clinical features












































































Syndrome Causative mutation Cutaneous features Extracutaneous features Associated malignancy
Tuberous sclerosis TSC1, TSC2 Hypomelanotic macules, angiofibromas, forehead plaques, shagreen patches, periungual fibromas Seizures, infantile spasms, intellectual disability.
Renal cysts and angiomyolipomas, cardiac rhabdomyomas
Malignant angiomyolipoma, renal cell cancer; sub-ependymal giant cell astrocytoma (SEGA)
Proteus Mosaic AKT1 Cerebriform connective tissue nevi (CCTN), epidermal nevi, vascular malformations, soft subcutaneous masses, patchy dermal hypoplasia, macrodactyly and lipomas Disproportionate, relentless segmental overgrowth of body parts; skeletal asymmetry, lung cysts, thromboembolism, eye problems, ovarian cysts, epididymal cysts.
Overgrowth generally after neonatal period
Mostly benign tumors
Hemihyperplasia-multiple lipomatosis (HH-ML) Unknown Superficial capillary vascular malformation, lipomas. Lacks deep vascular malformation and cerebriform connective tissue nevi of Proteus. Non-distorting overgrowth present at birth Risk for embryonal malignancies is unknown. Screening for Wilms tumor, adrenal cell carcinoma, hepatoblastoma is recommended
Megalencephaly-capillary malformation (MCAP) Mosaic PIK3CA Patchy capillary malformations; stretchy skin and joints Large brain, growth dysregulation, asymmetry, syndactyly, polydactyly, developmental delay, hypotonia, frontal bossing Mildly increased risk of cancer ; Wilms tumor, leukemia; meningioma reported
Mosaic overgrowth with fibroadipose hyperplasia (MOFH) Activating PIK3CA Lacks cutaneous features of Proteus Distorting or non-distorting, segmental overgrowth of muscles, skeleton and fibroadipose tissue that is present at birth Unknown
SOLAMEN PTEN Signs of Cowden: trichilemmoma, acral keratoses, oral papillomas. Lacks cerebriform connective tissue nevi of Proteus Features of Cowden: macrocephaly, breast and thyroid hamartoma Breast, thyroid, endometrial
CLOVES Activating PIK3CA Vascular anomalies, truncal lipomas, epidermal nevi. May be wrinkled skin on the palms and soles, but not CCTN of Proteus Non-progressive overgrowth at birth.
Overgrown feet, hands; ‘sandal gap’ toes, severe scoliosis; high vascular-flow masses; phlebectasia; thromboembolism
Unknown
Encephalocraniocutaneous lipomatosis (ECCL) Unknown, sporadic Nevus psiloliparus overlying lipomatous overgrowth; angiofibromas, connective tissue nevi cutis aplasia, nodular skin tags Proportionate, non-distorting overgrowth at birth. Ocular abnormalities, CNS lipomas, heart defects, lytic bone lesions, hypospadias, cryptorchidism, seizures, jaw osteomas Mostly benign tumors. Low-grade glioma reported
Beckwith–Wiedemann syndrome (BWS) Imprinting error affecting chromosomal region 11p15.5 Nevus flammeus, distinctive ear creases, posterior helical pits Abdominal wall defects (omphalocele), placental overgrowth, macrosomia, macroglossia, abnormal kidney, cardiomegaly, hypoglycemia Tumor risk increased, especially embryonal tumors; requires monitoring
Simpson–Golabi–Behmel syndrome type I Glypican-3 (GPC3) Supernumerary nipples, characteristic index finger and nail hypoplasia Macrosomia, macrocephaly, macroglossia, coarse square-shaped face, abdominal hernias, broad hands, normal intelligence Risk of embryonal tumors increased; requires monitoring
Sotos syndrome Nuclear receptor set domain containing protein 1 gene (NSD1) Frontotemporal sparse hairs, malar flushing Learning disabilities, distinct facies, macrocephaly, tall stature Overall cancer risk slightly increased. Age appropriate cancer screening recommended



Figure 29.6


PI3K-AKT pathway.

Activation of the PI3K-AKT pathway leads to cell growth and proliferation. PI3 Kinase (PI3K) is activated when bound to GTP-bound Ras and certain other ligands. PI3K activates AKT kinases. PTEN antagonizes the activity of PI3K and inhibits the pathway. PTEN also inhibits phosphoinositide-dependent kinase 1 (PDK) and other enzymes to inhibit the pathway. MCAP, megalencephaly-capillary malformation; MOFH, mosaic overgrowth with fibroadipose hyperplasia.



Figure 29.7


Proteus syndrome.

Hemihypertrophy and lipomatosis.

(Courtesy of Dr V.P. Sybert.)


PI3K-AKT activity is considered so essential that disruptive germline mutations are often presumed fatal. For example, an activating PI3K pathway mutation appears only in the mosaic form. In addition to impacting embryonic development, the PI3K-AKT pathway participates in normal cellular function by regulating glucose metabolism and apoptosis. Therefore, mutations affecting this pathway may cause congenital anomalies as well as ongoing complications. Improved understanding of the PI3K pathway, especially by revealing therapeutic targets for inhibitory drugs like rapamycin, gives hope for future trials and treatment.


Tuberous sclerosis


Tuberous sclerosis (TSC, MIM #191100) is a multisystem disorder characterized by tumors and hamartomas affecting the skin, brain, heart, kidneys and lungs, often in association with seizures and developmental delay ( Box 29.5 ). TSC is discussed in further detail in Chapter 23 .



Box 29.5

Clinical diagnostic criteria for tuberous sclerosis


Major features





  • Facial angiofibromas or forehead plaque



  • Nontraumatic ungual fibroma



  • ≥3 hypomelanotic macules



  • Shagreen patch



  • Multiple retinal nodular hamartomas



  • Cortical tuber a


    a Cerebral cortical dysplasia and cerebral white matter migration tracts count as one feature rather than two when they occur together.




  • Subependymal nodule



  • Subependymal giant cell astrocytoma



  • Cardiac rhabdomyoma



  • Renal angiomyolipoma or pulmonary lymphangiomyomatosis b


    b Other features of TSC must be present for a definite diagnosis when lymphangiomyomatosis and renal angiomyolipomas are both present.




Minor features





  • Multiple randomly distributed pits in dental enamel



  • Hamartomatous rectal polyps



  • Bone cysts



  • Cerebral white matter radial migration lines a



  • Gingival fibromas



  • Nonrenal hamartoma



  • Retinal achromic patch



  • ‘Confetti’ skin lesions



  • Multiple renal cysts



Diagnostic requirements





  • Definite diagnosis: two major features or one major and two minor features



  • Probable diagnosis: one major and one minor feature



  • Possible diagnosis: one major or two minor features




Cutaneous findings


There is a very high prevalence of cutaneous findings in TSC. Hypomelanotic macules are usually present at birth or appear within the first few months of life and ultimately are present in approximately 90% of TSC patients. Classically, they present as an ‘ash leaf macule,’ an oval area with reduction in pigment ( Fig. 29.8A ). These areas can also be irregular in outline and shape, or very small and guttate (confetti-like) ( Fig. 29.8B ). In fair-skinned infants, a Wood’s lamp examination may be necessary for detection. They can also occur on the scalp, with lightening of the hair within the patch. A single, hypopigmented macule in an infant, without other features of TSC, should not cause concern, but multiple lesions (≥3) should lead to further investigation.




Figure 29.8


Tuberous sclerosis.

(A) Ash leaf macules are often present at birth or noted early in infancy. (B) Confetti hypopigmentation typically becomes more common over time. (C) Facial plaque on the left upper cutaneous lip in a 3½-year-old child. (D) Shagreen patch: large shagreen patches may be congenital, whereas smaller ones typically develop over time. (E) Gingival fibromas are a less common feature, but occasionally develop in young children.










Classic facial angiofibromas typically appear after 4 years of age, however fibrous plaques resembling coalescence of angiofibromas may be present over the scalp, face, or neck at birth or appear shortly thereafter, as firm slightly raised patches or plaques that are commonly erythematous ( Fig. 29.8C ). Shagreen patches – firm, palpable thickened dermal plaques – can occur in the lumbar region as a roughened area of erythematous skin with a rubbery consistency or develop in other areas of the torso ( Fig. 29.8D ). They range in size from a few millimeters to 15 cm in diameter, and generally appear by adolescence but are infrequent in young infants. Periungual fibromas are similarly uncommon in the first decade. Gingival fibromas are a less common feature, but occasionally develop in young children ( Fig. 29.8E ).


Extracutaneous findings


Seizures occur in more than 60–80% of patients with TSC. Conversely 4–50% of infants with infantile spasms have TSC. TSC patients with early onset of seizures (<2 years of age) or infantile spasms have an elevated risk for intellectual disability. The most common lesions in the brain include tubers, subependymal nodules and subependymal giant-call astrocytomas (SEGA). Renal cysts, angiomyolipomas, and cardiac rhabdomyomas are findings in newborns and infants that suggest TSC. Cardiac rhabdomyomas are often discovered on routine antenatal ultrasound; 30–50% of infants with TSC have cardiac rhabdomyomas, and 80–90% of infants with these lesions have TSC. They are rarely symptomatic and typically regress spontaneously. An expert panel at the Tuberous Sclerosis Consensus Conference recommended a baseline electrocardiogram both at the time of diagnosis and prior to surgery, as cardiac rhabdomyomas can be associated with pre-excitation and arrhythmias on the electrocardiogram. Angiomyolipomas are the most common renal manifestation of TSC.


Etiology and pathogenesis


TSC may be caused by an autosomal dominant mutation in the TSC1 gene (encoding hamartin) or the TSC2 gene (encoding tuberin). The two proteins form a complex that is involved with the phosphoinositide-3-kinase (PI3K) signaling pathway, which regulates cell growth and proliferation ( Fig. 29.6 ).


Differential diagnosis


The differential diagnosis for the hypopigmented macules seen in the neonatal period includes vitiligo, nevus depigmentosus, nevus anemicus, and piebaldism. A single lesion, or several lesions occurring along the lines of Blaschko suggests the diagnosis of nevoid hypopigmentation rather than TSC (see Chapter 23 ). Connective tissue nevi may be sporadic and have also been associated with Buschke–Ollendorff or Proteus syndrome. Angiofibromas have been described in MEN1 and Birt–Hogg–Dubé syndrome, and also as an isolated autosomal dominant disorder.


Treatment and care


Consensus recommendations for screening and evaluation of TSC were proposed in 1998 and updated in 2000 ( Box 29.6 ). The Scottish Clinical Genetics Service and the UK Tuberous Sclerosis Association have also created clinical guidelines. Neurology and/or neurosurgery should be consulted for management of seizures, brain tumors, and shunting of obstructive hydrocephalus. Ophthalmology should also examine patients to assist in confirming the diagnosis. Renal ultrasound or renal MRI are important to screen angiomyolipomas. This may also help to identify patients with coexisting polycystic kidney disease due to a contiguous gene deletion syndrome involving the TSC2 and PKD1 genes. Echocardiography and electrocardiogram are recommended at diagnosis for confirmation (to detect cardiac rhabdomyomas and arrhythmias) and to screen for aortic aneurysms.



Box 29.6

Care plan for tuberous sclerosis

Testing recommendations in the neonate or infant at time of diagnosis





  • Age-appropriate neurologic and developmental assessment



  • Dermatologic examination



  • Ophthalmic examination



  • Neurologic consultation



  • Cardiac evaluation (ECG and echocardiogram)



  • Renal MRI or renal ultrasound



  • Head magnetic resonance imaging



  • Additional information for recommended screening, and surveillance and management can be found at: www.tsalliance.org/pages.aspx?content=731 (Accessed February 2014)




Pulsed dye laser has been recommended for flat erythematous angiofibromas, and both Potassium titanyl phosphate (KTP) laser and carbon dioxide laser are used to treat more elevated lesions, but are rarely indicated in infants. Fibrous forehead plaques are generally left untreated, but may also be treated with lasers or surgery. Several case reports have recently described the utility of topical rapamycin for the treatment of angiofibromas. This approach holds promise, but further study is needed to establish the safety, efficacy and dosing guidelines.


Proteus syndrome


Proteus syndrome (MIM #176920) is a very rare condition characterized by dramatic segmental or mosaic overgrowth. Common complications include skeletal asymmetry, characteristic overgrowth of the palms or soles referred to as ‘cerebriform connective tissue nevi’ (CCTN), linear epidermal nevi, deep or superficial vascular malformations, dysregulated adipose tissue (formerly referred to as lipomas) and tumor predisposition (see also Chapter 22 ).


Cutaneous findings


Almost all individuals with Proteus syndrome have a dermatologic manifestation. Over 40% of affected neonates will demonstrate at least some evidence of the disease at birth, such as epidermal nevi or vascular malformations. The three main cutaneous findings are epidermal nevi, vascular malformations, and soft subcutaneous masses. Epidermal nevi are usually linear and verrucous, but may be macular and hyper- or hypopigmented. Malformations may be venous, capillary, and/or lymphatic. The cerebriform connective tissue nevus, when on the sole of the foot, is caused by hyperplasia of cutaneous and subcutaneous tissues and considered virtually pathognomonic. The tissue is very firm; similar lesions may also occur on the hands, perinasal area, or near the canthus. Prominent cutaneous venous structures may occur as a result of patchy dermal hypoplasia. Macrodactyly and adipose overgrowth may also be observed.


Extracutaneous findings


Overgrowth in Proteus syndrome is disproportionate, asymmetric, progressive, distorting, and persistent (see Fig. 29.7 ). Overgrowth usually presents between 6 and 18 months of age and can occur in areas that were completely normal at birth. Overgrowth affects most tissues including bones, cartilage, muscle, and connective tissues. At least some overgrowth and asymmetry is present at birth in 17.5% of cases. Orifices may be affected, causing respiratory obstruction, conductive hearing loss, or gastric outlet obstruction. Cystic degeneration of the lungs may lead to pneumonia. Affected individuals are predisposed to deadly deep venous thrombosis and pulmonary embolism. The central nervous system is commonly affected by hemimegalencephaly (unilateral enlargement of the brain), but most patients are asymptomatic. Eye complications are common and range from strabismus to epibulbar hamartomas. Ovarian cystadenomas and cystic lesions of the epididymis are also common.


Etiology and pathogenesis


The cause of Proteus syndrome is a de novo post-zygotic activating mutation in the AKT1 oncogene. Proteus features are an example of somatic mosaicism that is lethal in the non-mosaic state. Because Proteus is a mosaic disorder, biopsy of affected tissue is required to make a genetic diagnosis.


Differential diagnosis


Proteus syndrome has been overdiagnosed, prompting the creation of diagnostic criteria ( Box 29.7 ) to separate Proteus syndrome from other overgrowth syndromes, many of which share asymmetric hypertrophy as a feature but almost always to a less severe degree. Proteus stands apart by having fairly rapid postnatal progression, relentless deforming overgrowth and a poor prognosis.



Box 29.7

Diagnostic criteria for Proteus syndrome


General criteria: Mosaic, and progressive, and sporadic


Category A: Cerebriform connective tissue nevus


Category B:



  • 1.

    Epidermal nevus


  • 2.

    Disproportionate overgrowth in one: limbs, skull, external auditory canal, vertebrae, or viscera


  • 3.

    Bilateral ovarian cystadenomas or monomorphic adenomas of the parotid gland in children



Category C:



  • 1.

    Dysregulated adipose tissue (lipoatrophy or lipomas)


  • 2.

    Vascular malformations (capillary, venous, or lymphatic)


  • 3.

    Facial phenotype, all: long face, dolichocephaly, downslanting palpebral fissures, low nasal bridge, wide or anteverted nares, open mouth at rest



All three general criteria plus either one from A, two from B, or three from C are required to make a diagnosis of Proteus syndrome.



Hemihyperplasia-multiple lipomatosis (HH-ML).


This is most commonly misdiagnosed as Proteus syndrome. HH-ML includes superficial capillary vascular malformation (similar to port-wine stain), but lacks progressive, distorting overgrowth, deep vascular malformations and cerebriform connective tissue nevi on the palms or soles. In non-distorting overgrowth that characterizes HH-ML, a bone is normally shaped and larger than expected, but without growths or odd edges. In HH-ML, non-distorting overgrowth is present at birth, whereas, the distinctive distorting overgrowth that characterizes Proteus may not be apparent until age 2 or 3. Lipomas may recur after surgical removal. Therefore, removal of symptomatic lipomas only is recommended.


Megalencephaly-capillary malformation (MCAP).


Sometimes also referred to as M-CM, it has previously been termed macrocephaly-capillary malformation and macrocephaly-cutis marmorata telangiectatica congenital. MCAP sometimes includes markedly large brain size with variable cortical malformation, growth dysregulation with variable asymmetry, patchy capillary malformations frequently on the philtrum, upper lip and nose as well as the limbs and trunk, and distal limb abnormalities such as syndactyly and polydactyly, and mild connective tissue dysplasia (hyperextensible joints and skin). Congenital Chiari I malformation had been associated with MCAP, however, the term ‘cerebellar tonsil herniation’ (CTH) is now preferred to describe acquired herniation caused by cerebellar overgrowth that occurs in up to 70% of MCAP cases. With capillary vascular malformation and asymmetric overgrowth, children often meet the criteria for Klippel–Trenaunay syndrome. Affected children typically have developmental delay (85%) and neonatal hypotonia (68%). Frontal bossing and prominent nevus simplex are additional facial features. There is also a mildly increased risk of cancer (about 3%). MCAP has been associated with postzygotic mutations in the PIK3CA gene.


Mosaic overgrowth with fibroadipose hyperplasia (MOFH).


This is an example of an overgrowth syndrome defined by its newly identified causative mutation, an activating mutation in the PIK3CA gene. Affected children have segmental overgrowth that affects the muscles, skeleton, and fibroadipose tissue without cutaneous features of Proteus syndrome. Both distorting and non-distorting overgrowth are reported. The features of MOFH often begin at birth, in contrast to Proteus syndrome which generally appears later.


SOLAMEN syndrome.


Segmental overgrowth, lipomatosis, arteriovenous malformation and epidermal nevus (SOLAMEN) is a ‘Proteus-like’ syndrome, now known to be a mosaic form of Cowden disease. Affected individuals carry a germline PTEN mutation and a mosaic second hit to the PTEN gene on the opposite allele in affected tissues. Absence of the cerebriform connective tissue nevi on the palms and soles distinguishes SOLAMEN syndrome. In addition, characteristic features of Cowden disease such as macrocephaly, breast and thyroid hamartomas and skin changes are likely to be present.


CLOVES syndrome (MIM #612918).


Congenital lipomatosis, overgrowth, vascular malformations, epidermal nevi and skeletal anomalies (CLOVES) describes another subset of patients, most of whom were initially misdiagnosed with Proteus syndrome. In CLOVES syndrome, overgrowth is present at birth with truncal vascular anomalies, truncal lipomatous masses and overgrown feet with acral or musculoskeletal anomalies. In contrast to Proteus, the overgrowth is not progressive. Patients may have wrinkled skin on the palms and soles, but lack the firm rubbery CCTN of Proteus syndrome. Since CLOVES syndrome was suspected to be a mosaic disorder at the outset, massive DNA sequencing of affected tissues revealed causative activating mutations in PIK3CA . Severe scoliosis, large truncal masses, high flow vascular lesions, phlebectasia with thromboembolism and orthopedic problems of the hands and feed may all require early, aggressive intervention in affected individuals. Prognosis seems better compared to Proteus syndrome but this condition can still be very severe, even life-threatening.


Encephalocraniocutaneous lipomatosis (ECCL).


The so-called ‘nevus psiloliparus’ is the cutaneous hallmark, with a localized non-scarring patch of alopecia on the scalp which may or may not overlie a fatty tissue mass. ECCL, while once thought to be a localized form of Proteus syndrome, does not meet the diagnostic criteria of Proteus, lacking disproportionate growth as a salient feature (see also Chapter 31 ).


Differential diagnosis of Proteus and similar disorders


Maffucci syndrome consists of multiple enchondromatosis (which may be confused with hyperostosis) and vascular malformations. Klippel–Trenaunay (MIM #149000) syndrome consists of vascular malformations with overgrowth, typically in the same segment. Axillary freckling and neurofibromas help distinguish neurofibromatosis.


Management


Management of these syndromes depends on the specific disease; if overgrowth is severe – as in Proteus syndrome – management is often very difficult. A multidisciplinary approach best addresses all aspects of the disease adequately. Ongoing ophthalmology, neurology, and developmental assessment exams are recommended. Caregivers should be informed of the risk of pulmonary embolism and stroke so that healthcare providers consider it if an emergency arises. Orthopedic surgery should be consulted before functional deficits appear and before the patient becomes too debilitated to undergo surgery. Cancer surveillance is an important part of management as dictated by clinical symptoms; routine imaging is not recommended.


Isolated hemihyperplasia places individuals at increased risk (5.9%) for embryonal malignancies such as Wilms tumor, adrenal cell carcinoma and hepatoblastoma. A study of 260 children with hemihyperplasia reported that the risk in truly isolated idiopathic hemihyperplasia is lower (1.2%) and in syndrome-related hemihyperplasia higher (10%) than previously reported. The risk of malignancy in specific syndromes with hemihyperplasia, including HH-ML and excluding Klippel–Trenaunay, is not clear. Until further information becomes available, screening with abdominal ultrasound every 3–6 months until age 8, checking of blood alpha fetoprotein level every 3 months until age 4 and referral to a geneticist for identifying associated syndromes is recommended. Individuals with SOLAMEN syndrome have a risk of malignancies associated with Cowden (PTEN hamartoma) syndrome.




Additional overgrowth syndromes


Of the generalized overgrowth syndromes, Beckwith–Wiedemann Syndrome (BWS) (MIM #130650) is the most common. Cutaneous features include prominent nevus simplex, distinctive anterior ear creases, and posterior helical pits. Other characteristic features are abdominal wall defects (omphalocele), placental overgrowth, macrosomia, macroglossia, kidney abnormalities, cardiomegaly, and hypoglycemia. As the phenotype is variable, mild cases are likely to be missed. Mosaicism may lead to asymmetric hypertrophy of a limb or body part. BWS patients have an increased risk of Wilms tumor and hepatoblastoma.


Beckwith–Wiedemann is a disorder of imprinting, an epigenetic process using methylation to silence either the maternal or paternal allele in a gene pair. Imprinting affects only specific regions of the genome, especially areas with genes impacting fetal growth. Beckwith–Wiedemann syndrome affects chromosomal region 11p15.5. This region contains an imprinting center that regulates several adjacent genes. Since 15% of cases are inherited, siblings are considered at risk for the disorder and require screening for complications. Monitoring for neonatal hypoglycemia, for example, may prevent neurologic injury. Affected children may benefit from tongue reduction surgery and speech therapy. Surveillance for abdominal embryonal tumor (described above) with ultrasound and blood testing and ongoing screening for renal abnormalities is recommended.


Simpson–golabi–behmel syndrome type I


Simpson–Golabi–Behmel syndrome type I is an overgrowth syndrome with cutaneous features including supernumerary nipples and dysplastic fingernails. The index fingers are affected with hypoplasia and nail abnormality and this characteristic feature may help in early diagnosis ( Fig. 29.9 ). Extracutaneous features are macrosomia, macrocephaly, macroglossia, coarse square-shaped face, abdominal hernias, broad hands, and normal intelligence. The X-linked recessive disorder is caused by a mutation in glypican-3 (GPC3) gene. Risk of embryonal tumors is increased and requires monitoring.




Figure 29.9


Simpson–Golabi–Behmel syndrome type I.

Shortened and widened hand, post-axial polydactyly and a hypoplastic index finger (partially hidden) with absent nail in an affected 6-month-old infant.

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Jul 23, 2019 | Posted by in PEDIATRICS | Comments Off on Selected Hereditary Diseases
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