2019•StatPearlsRequires access

Androgen Insensitivity Syndrome

Shikha Singh, Stella Ilyayeva

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Abstract

Androgen insensitivity syndrome (AIS) is a common etiology of sexual developmental disorders resulting in varying phenotypes. These disorders of androgen action present as 46 XY disorders or differences of sex development (DSD). The phenotypic spectrum of AIS depends on the residual androgen receptor activity and encompasses individuals with completely female phenotype to male phenotype with infertility /undervirilization . Androgen resistance results in complete androgen insensitivity syndrome (CAIS) characterizing XY sex reversal with normal female phenotype whereas phenotype diversity is variable with residual androgen receptor activity which leads to partial androgen insensitivity syndrome (PAIS). PAIS presents a substantial challenge to the clinician in determining the gender identity at the time of the birth of the child. Therefore, it is crucial for the clinician to have an understanding of the physiology of androgen receptors mechanism to diagnose the condition as CAIS or PAIS accurately and plan the treatment course from birth to adulthood.

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What this paper is about

Androgen insensitivity syndrome (AIS) is a common etiology of sexual developmental disorders resulting in varying phenotypes. These disorders of androgen action present as 46 XY disorders or differences of sex development (DSD). The phenotypic spectrum of AIS depends on the residual androgen receptor activity and encompasses individuals with completely female phenotype to male phenotype with infertility /undervirilization . Androgen resistance results in complete androgen insensitivity syndrome (CAIS) characterizing XY sex reversal with normal female phenotype whereas phenotype diversity is variable with residual androgen receptor activity which leads to partial androgen insensitivity syndrome (PAIS). PAIS presents a substantial challenge to the clinician in determining the gender identity at the time of the birth of the child. Therefore, it is crucial for the clinician to have an understanding of the physiology of androgen receptors mechanism to diagnose the condition as CAIS or PAIS accurately and plan the treatment course from birth to adulthood.

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Available abstract

Androgen insensitivity syndrome (AIS) is a common etiology of sexual developmental disorders resulting in varying phenotypes. These disorders of androgen action present as 46 XY disorders or differences of sex development (DSD). The phenotypic spectrum of AIS depends on the residual androgen receptor activity and encompasses individuals with completely female phenotype to male phenotype with infertility /undervirilization . Androgen resistance results in complete androgen insensitivity syndrome (CAIS) characterizing XY sex reversal with normal female phenotype whereas phenotype diversity is variable with residual androgen receptor activity which leads to partial androgen insensitivity syndrome (PAIS). PAIS presents a substantial challenge to the clinician in determining the gender identity at the time of the birth of the child. Therefore, it is crucial for the clinician to have an understanding of the physiology of androgen receptors mechanism to diagnose the condition as CAIS or PAIS accurately and plan the treatment course from birth to adulthood.

Key concepts: Androgen receptor, Androgen insensitivity syndrome, Complete androgen insensitivity syndrome, Androgen, Phenotype, Etiology, Sexual differentiation, Disorders of sex development

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