Normal Sexual Development

The normal development of the reproductive organs in humans begins with the differentiation of primordial structures and ends with the completion of secondary sexual characteristics that begins during puberty (see Chapter 67 for a discussion on puberty). Around the fifth week of gestation, the genital ridge develops into the appropriate gonads based on the chromosomal sex (XX or XY) established at conception. A complex series of genetic events must occur to establish the appropriate differentiation to an ovary or testis. It was clear that genes on the Y chromosome were involved in this differentiation because the presence of a Y chromosome resulted in male sexual characteristics, such as in XY or XXY individuals. Before these genes were known, they were referred to as “testis-determining factor” (TDF) because their presence led to testis formation. Ovaries and other female-specific reproductive organs were believed to develop by “default” because of the absence of Y chromosome material or TDF. Accordingly, research in mice and humans with X-Y translocations determined that the SRY gene (sex-determining region, Y) encoded for a transcription factor that is necessary for male reproductive organ development. Additional genes have also been identified for testis formation (Figure 119-1), and mutations in any of these genes (e.g., SOX9, DMRT1) have been associated with sex-reversal in XY patients. It is also important to note that more recent data have demonstrated an active role of several genes (FOXL2, WNT4, RSPO1) in ovary development in XX individuals, contradicting the older “default” female development notion.

Figure 119-1 Genes associated with testicular and ovarian differentiation.

After the development of the gonads, the genital ducts must differentiate into the appropriate internal structures necessary for reproduction (Figure 119-2). In the undifferentiated stage, both mesonephric (Wolffian) and paramesonephric (Müllerian) ducts are present. In males, the newly formed testes secrete anti-Müllerian hormone (AMH), inhibin B, and testosterone between weeks 7 and 11, causing the Müllerian ducts to regress and the Wolffian ducts to persist, eventually becoming the seminal vesicles, vas deferentia, and epididymis. The opposite occurs in females, in whom the absence of testicular secretions causes the mesonephric ducts to regress and the Müllerian ducts to persist, forming the fallopian tubes, uterus, and upper third of the vagina

Figure 119-2 Gonad and genital duct formation.

The undifferentiated genital tubercle, labioscrotal swellings, and urethral folds are present around gestational week 4, and the external genitalia begin to become more distinguishable during weeks 9 to 13. In males, the presence of testosterone and the testosterone derivative dihydrotestosterone (converted by 5-αreductase) causes the genital tubercle to form the glans penis, stimulating the urethral folds to fuse ventrally and form the spongy urethra and resulting in part of the penile shaft and labioscrotal swellings to fuse and form the scrotum (Figure 119-3). The absence of testosterone and dihydrotestosterone in females causes the genital tubercle to form the glans clitoris and the urethral folds and labioscrotal swelling to remain unfused (except posteriorly) to form the labia minora and labia majora, respectively. In males, testicular descent begins during the twelfth week of gestation and finishes during the third trimester.

Figure 119-3 Differentiation of external genitalia.

Etiology, Pathogenesis, and Clinical Presentation

Because of the myriad genes associated with urogenital development, many genetic abnormalities may alter the structure and function of the reproductive organs. As noted above, these DSDs have been recently subtyped into sex chromosome DSDs, 46,XY DSDs, and 46,XX DSDs (Table 119-1). Sex chromosome DSDs are caused by various mechanisms (Figure 119-4) and include Klinefelter syndrome (47,XXY) and variants, Turner syndrome (45,X) and variants, and other types of XX/XY mosaicism, as discussed in Chapter 118, and typically result in largely normal prenatal sexual development but reduced function of the gonads during and after puberty. Most other genetic abnormalities may include point mutations, frameshift mutations, or deletions of specific genes that cause the protein product to be nonfunctional and thereby affect gonad differentiation, leading to a disparity between the chromosomal sex (XX or XY) and gonad development (ovary or testis).

Table 119-1 Classification of Disorders of Sexual Differentiation

Figure 119-4 Errors in chromosomal sex.