Androgen insensitivity syndrome (https://homosaurus.org/v3/homoit0000044)




Identificador
homoit0000044
Etiqueta preferida
Androgen insensitivity syndrome
English
Etiqueta alternativa
AIS
English
Goldberg-Maxwell syndrome
English
Male androgen insensitivity syndrome
English
Descripción
People born with AIS have XY chromosomes and testes, and their bodies have varying levels of insensitivity to androgens (including testosterone). This means that their cells do not respond typically to the testosterone that they produce. Like other variations in sex characteristics, AIS is a spectrum, with the subcategories of complete (CAIS), partial (PAIS), and mild androgen insensitivity (MAIS). The term "male androgen insensitivity syndrome" should not be used to describe this variation because many people with AIS are women.
English
Nota histórica
Term updated in collaboration with interACT: Advocates for Intersex Youth, 2022-2023.
English
Colaboradores
Revised during an extended collaboration with interACT: Advocates for Intersex Youth, 2022-2023.
English
Issued (Created)
2019-05-14 07:03:46 UTC
Modified
2021-12-08 09:28:13 UTC
Más amplio
Intersex variations [homoit0000669]
Más específico
Complete gonadal dysgenesis [homoit0002830]
Mild androgen insensitivity syndrome [homoit0002866]
Partial androgen insensitivity syndrome [homoit0001079]
Replaces
http://homosaurus.org/v2/androgenInsensitivitySyndrome

Visualización de jerarquía

Intersex variations
Androgen insensitivity syndrome
Partial androgen insensitivity syndrome
Complete gonadal dysgenesis
Mild androgen insensitivity syndrome


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