Androgen insensitivity syndrome classification
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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
- Based on the degree of genital masculinization, Androgen insensitivity syndrome is divided into three categories: [1]
- When the external genitalia is that of a normal female it is classified as Complete androgen insensitivity syndrome (CAIS)
- When the external genitalia is that of a normal male it is classified as Mild androgen insensitivity syndrome (MAIS)
- When the external genitalia is partially, but not fully masculinized it is classified as Partial androgen insensitivity syndrome (PAIS)
- Individuals with both Partial androgen insensitivity syndrome (PAIS) and Complete androgen insensitivity syndrome (CAIS) have 46 XY karyotypes.
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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References
- ↑ Bhaskararao G, Himabindu Y, Nayak SR, Sriharibabu M (2014). "Laparoscopic gonedectomy in a case of complete androgen insensitivity syndrome". J Hum Reprod Sci. 7 (3): 221–3. doi:10.4103/0974-1208.142498. PMC 4229800. PMID 25395750.