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Androgen insensitivity syndrome

Androgen insensitivity syndrome (AIS), also known as testicular feminization, is one of the most common conditions where the chromosome sex and gonadal sex do not agree with the phenotypic sex. Affected people have normal male chromosomes, 46,XY and testicles. The testicles secrete both testosterone and mullerian duct inhibitor as normal and no internal female structures form. However, due to defective androgen receptors, the wolffian ducts and genitals cannot respond to the androgens testosterone and dihydrotestosterone. As a result, no male internal structures are formed from the wolffian ducts and the external genitals are feminized.

The amount of feminization depends on the severity of the androgen receptor defect and is often characterized as complete androgen insensitivity (CAIS), partial androgen insensitivity (PAIS), and mild androgen insensitivity (MAIS). In complete androgen insensitivity, the alteration in the androgen receptor results in complete female

Classification of AIS Phenotypes
Type External genitalia (synonyms) Findings
CAIS Female (“testicular feminization”) Absent or rudimentary wolffian duct derivatives
    Inguinal or labial testes; short blind-ending vagina
    Little or no pubic and/or axillary hair
CAIS or PAIS Predominantly female (incomplete AIS) Inguinal or labial testes
    Labial fusion and enlarged clitoris
    Distinct urethral and vaginal openings or a urogenital sinus
PAIS Ambiguous Microphallus (<1 cm) with clitoris-like underdeveloped glans; labia majora-like bifid scrotum
    Descended or undescended testes
    Perineoscrotal hypospadias or urogenital sinus
    Excessive development of the male breasts during puberty
  Predominantly male Simple (glandular or penile) or severe (perineal) “isolated” hypospadias with a normal-sized penis and descended testes or severe hypospadias with micropenis, bifid scrotum, and either descended or undescended testes
    Excessive development of the male breasts during puberty
MAIS Male (undervirilized male syndrome) Impaired sperm development and/or impaired masculinization
    Overdevelopment of the male breasts during puberty

external genitals. In partial androgen insensitivity, also called Reifenstein syndrome, partial androgen insensitivity results in female genitalia with some masculinization, ambiguous genitalia, or male genitalia with partial feminization. With mild androgen insensitivity, mild androgen resistance results in normal male genitals or a male with mild feminization.

In both CAIS and PAIS, affected individuals are sterile (can not have a child). In MAIS, the affected male may have fertility problems because of oligospermia, low sperm production, or azoospermia, no sperm production. In all types of AIS, secondary sex characteristics such as body and pubic hair can be abnormal. Mental impairment is not found in any of the types of androgen insensitivity syndromes, though poor visual-spatial ability has been observed. People with AIS can also be rather tall, though bone age is usually normal.

Definition

Androgen insensitivity syndrome is a genetic condition where affected people have male chromosomes and male gonads (testicles). The external genitals, however, have mild to complete feminization.

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Author Info: Carin Lea Beltz MS, CGC, The Gale Group Inc., Gale, Detroit, Gale Encyclopedia of Genetic Disorders Part I, 2002
 
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