Circuit G

Circuit G



STATION 1


This station assesses your ability to elicit clinical signs:







STATION 2


This station assesses your ability to elicit clinical signs:







STATION 3


This station assesses your ability to elicit clinical signs:







STATION 4


This station assesses your ability to elicit clinical signs:








STATION 6


This station assesses your ability to assess specifically requested areas in a child with a developmental problem:






CLINICAL SCENARIO


The infant is accompanied by her mother. On initial general inspection you find her to be looking around lying on her back. She is moving all four limbs, is able to reach out for bright toys, pass objects from hand to hand and to place them in her mouth. She turns to her mother’s voice but makes little noise and no words herself.


You ask the mother if you may examine her more closely. With permission you then formally test the motor development (gross and fine motor).


On pulling to sit there is reduced truncal tone and mildly reduced head control. She is unable to sit unsupported. When held vertically, she will put weight on both legs and bounce weakly. She will not support herself or hold on to the cot side for support. In ventral suspension you again note impaired head control (to 45°) and truncal hypotonia. On lying her down on her front the infant will push on her hands a limited amount. You move on to test the Moro reflex, which has been lost.


You test fine motor control initially with a single bright red brick, which she takes in a full palmar grasp and transfers from hand to hand. A second brick is introduced, which she takes in her other hand and then bangs the bricks together. She is not able to scribble with a crayon, build blocks into a tower of three or put pieces into a simple jigsaw.


What is the developmental age of this child in the area of gross motor development?


What is the developmental age of this child in the area of fine motor development?


What additional developmental reflexes could you describe or test in this child?



STATION 7


This station assesses your ability to communicate appropriate, factually correct information in an effective way within the emotional context of the clinical setting:








STATION 8


This station assesses your ability to communicate appropriate, factually correct information in an effective way within the emotional context of the clinical setting:








STATION 9


This station assesses your ability to take a focused history and explain to the parent your diagnosis or differential management plan:






COMMENTS ON STATION 1



DIAGNOSIS: REPAIR OF AORTIC COARCTATION; TURNER’S SYNDROME


A thorough knowledge of cardiovascular defects, their management and their sequelae is vital for the exam. It is important that you know what the common scars look like – reading about a lateral thoracotomy scar is not the same as having seen one. In this case the small secondary scar is probably from a chest drain.


It is important to let the examiner know that you would measure a four- limb BP in addition to plotting the length, weight and head circumference on the appropriate chart. An ECG, CXR and echocardiogram are essential firstline investigations of a significant murmur with no innocent features.


This child has had a repair of aortic coarctation; the pedal oedema is important as it suggests an underlying diagnosis of Turner’s syndrome. It is not a feature of cardiac failure in this circumstance. Karyotyping of a blood sample will be diagnostic in the majority of cases.


The clinical features of Turner’s syndrome (congenital lymphoedema, short stature and gonadal dysgenesis) can be divided into neonatal, childhood and adolescent findings. You should become familiar with Turner’s syndrome as the children are generally well but require prolonged follow-up. Extensive detail is provided here as this same child could be used for the communication skills stations – ‘Explain to this child’s parents what a diagnosis of Turner’s syndrome means?’ – or as a history-taking/ management-planning scenario.






































































Age Clinical findings
Neonatal Dorsal oedema of hands and feet
  Redundant nuchal skin folds (secondary to in utero cystic hygromas)
  Low birth weight and reduced length
  17-45% cardiac lesion (bicuspid aortic valve, coarctation of aorta, aortic stenosis, hypoplastic left heart)
  Developmental dysplasia of the hip (DDH) more common
Childhood Short stature (proportional)
  10% developmental delay
  Facial abnormalities (epicanthic folds, small mandible, prominent ears, high palate)
  Webbed neck
  Low posterior hairline
  Prominent ‘shield’ chest
  Widely spaced nipples
  Cubitum valgum
  Hyperconvex fingernails
  Grommits for ‘glue ear’ common
Teenage Failed onset of pubertal development (10% have breast enlargement)
  Progressively more prominent pigmented naevi
  30% renal abnormalities
  70% impairment of non-verbal perceptual motor and visuospatial skills
  15-30% hypothyroid
  Scoliosis, lordosis and kyphosis more common

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Feb 14, 2017 | Posted by in PEDIATRICS | Comments Off on Circuit G

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