Androgen insensitivity syndrome classification: Difference between revisions
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==Overview== | ==Overview== | ||
Androgen insensitivity syndrome (AIS) represents a spectrum of defects in androgen action and can be subdivided into three broad phenotypes such as CAIS. PAIS and MAIS. | |||
==Classification== | ==Classification== |
Revision as of 11:43, 13 July 2017
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Aravind Reddy Kothagadi M.B.B.S[2]
Overview
Androgen insensitivity syndrome (AIS) represents a spectrum of defects in androgen action and can be subdivided into three broad phenotypes such as CAIS. PAIS and MAIS.
Classification
Androgen insensitivity syndrome (AIS) represents a spectrum of defects in androgen action and can be subdivided into three broad phenotypes:[1]
- Complete androgen insensitivity syndrome (CAIS), with typical female external genitalia
- Partial androgen insensitivity syndrome (PAIS) with predominantly female, predominantly male, or ambiguous external genitalia
- Mild androgen insensitivity syndrome (MAIS) with typical male external genitalia
Classification of Androgen Insensitivity Syndrome Phenotypes | ||
Type | External Genitalia | Findings |
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CAIS - (Complete androgen insensitivity syndrome) | Female (“testicular feminization”) |
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Predominantly female (“incomplete AIS”) |
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PAIS - (Partial androgen insensitivity syndrome) | Ambiguous |
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Predominantly male |
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MAIS - (Mild androgen insensitivity syndrome) | Male (“undervirilized male syndrome”) |
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