Handbook of Clinical Gender Medicine. Группа авторов
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Название: Handbook of Clinical Gender Medicine

Автор: Группа авторов

Издательство: Ingram

Жанр: Зарубежная психология

Серия:

isbn: 9783805599306

isbn:

СКАЧАТЬ of a bladder and urethra separate from the vagina requires the growth of a membrane from the cranial to the caudal region in the urogenital sinus. Anomalies of female embryogenesis during this process lead to a variety of clinically recognized disorders. Estrogen is responsible for the vascularity and thickness of vaginal tissue. Failure of the labia to fuse in the normal female fetus may be due in part to the lack of fetal androgen production and low 5-α reductase activity (and in part to maternal estrogen stimulation of ER-positive urethral folds), causing the labia minora to diverge laterally. There is extensive circumstantial evidence that 17β-estradiol and progesterone influence the postnatal physiology of extragenital and especially genital (vulval) skin in the human female.

      Molecular Biology

      The role of androgens in sexual differentiation was first elucidated in 1940 by Jost [2] who concluded that the testes were responsible for external genital differentiation through secretion of androgens. Recent studies have shown that androgen-related effects in a cell or tissue may be regulated through paracrine signaling by neighboring cells. In male genital differentiation in particular, the prostate demonstrates mesenchymal (stromal)-epithelial interactions that appear to be an integral part of the epithelium’s differentiation into characteristic branched ducts of the prostate. Steroid hormones such as 17β-estradiol and progesterone are capable of altering epithelial proliferation and organization through paracrine signaling of stromal cells. This paracrine signaling appears to be influenced by steroid-steroid hormone receptor interaction in the nearby cells.

      There is also evidence that androgens have direct, non-AR-regulated effects on cells. Direct intracellular response to androgens can occur quickly, within seconds to minutes. This so-called ‘nonclassical’ androgen response pathway can involve several mechanisms such as activation of sex hormone-binding globulin receptors, activation of phosphatidylinositol 3-OH kinase (PI3-K) signaling, and modulation of voltage-and ligand-gated ion channels and transporters. The idea that the role of AR extends beyond the classic androgen-AR mechanism of transcription regulation is intriguing in partial androgen insensitivity syndrome (PAIS). It is possible the varied phenotypical presentations seen in PAIS are in part related to other cellular signaling roles separate from AR that androgens play in genital differentiation.

      Classification of Ambiguous Genitalia

      Chromosomal Disorders

      Sex Reversal, Turner’s Syndrome, True Hemaphroditism, Mosaics, Mixed Gonadal Dysgenesis, and Pure Gonadal Dysgenesis. 46, XY sex reversal is a DSD resulting in individuals of the 46, XY genotype with female phenotypic characteristics or ambiguous genitalia and associated complete gonadal dysgenesis in ~1/20,000 births. The commitment of undifferentiated gonads to testes initiates the development into the male phenotype in normal 46, XY males. The Y chromosome has long been thought to carry the testis-determining factor (TDF). In the absence of the Y chromosome, such as in 46, XX normal females or 45, X Turner’s syndrome, the individuals are phenotypically female. The SRY is located at Yp11.3 and it was hoped that the discovery of SRY would lead to a rapid expansion of knowledge regarding early sex determination. However, SRY as the only TDF was shown to be a gross oversimplification. Many other genes active in sex differentiation have been confirmed, including genes coding for transcription factors such as SOX9 [Sry-type high-mobility group (HMG) box 9], DMTR1, GATA4, DAX1, SF1, WT1, LHX9, and DSS and signaling molecules antimullerian hormone (AMH), WNT4, FGF9, and DHH. Genes coding for the male phenotype have been found on X chromosomes (e.g. DSS) and autosomes 9, 10, and 17 (e.g. DMTR1).

      Genetic mutations at the distal end of the short arm of chromosome 9 have been demonstrated in cases of 46, XY sex reversal. Namely, doublesex and MAB-3 related transcription factors 1 (DMRT1) and 2 (DMRT2) are mapped to band 9p24.3. DMRT1 appears to play a role in early sex differentiation while the role of DMRT2 is in somitogenesis. Genetic mutations at the distal 9p locus are typically de novo, resulting from deletions at 9p more often than point mutations. The shortest deletion at 9p still results in the loss of both DMRT1 and DMRT2, allowing for the possibility of both playing a role in early sex determination. This may also account for multiple phenotypic anomalies seen in association with XY sex reversal in certain individuals with 9p mutations. Individuals with 9p mutations and XY sex reversal have been observed to display abnormal facies, hypotonia, and cardiac and gastrointestinal defects, as well as mental and motor developmental delay.

      Overvirilized Females

      Fetal Sources and Congenital Adrenal Hyperplasia

      Maternal or Exogenous Sources of Androgens

      Other sources of masculinization with resultant ambiguous genitalia are androgenic stimulation of the fetus in utero from nonfetal sources. Fetal virilization occurs during a critical period between weeks 8 and 13 of gestation and results in labioscrotal fusion and urogenital sinus formation. Female embryos have the same androgen receptor system in the urogenital tract as male embryos; therefore, administration of androgens at the appropriate time during embryogenesis may cause profound masculinization. Internal genitalia are not masculinized and wolffian duct remnants are normal.

      Although CAH is the most common cause of masculinization in the female fetus, masculinization as a consequence of a maternal СКАЧАТЬ