Androgen Insensitivity Syndrome: A rare genetic disorder

BACKGROUND: Androgen Insensitivity Syndrome (AIS) is a rare X-linked recessive androgen receptor (AR) disorder with 46XY karyotype. Partial AIS affects 5–7 per 1,000,000 genetically male individuals whereas Complete AIS affects 2–5 per 100,000 genetically male individuals. CAIS CAIS is characterized...

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Detalles Bibliográficos
Autores principales: Fulare, Sushrut, Deshmukh, Satish, Gupta, Jyoti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7322742/
https://www.ncbi.nlm.nih.gov/pubmed/32493623
http://dx.doi.org/10.1016/j.ijscr.2020.01.032

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7322742/
https://www.ncbi.nlm.nih.gov/pubmed/32493623
http://dx.doi.org/10.1016/j.ijscr.2020.01.032

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