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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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| Publicat a: | Int J Surg Case Rep |
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| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Elsevier
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7322742/ https://ncbi.nlm.nih.gov/pubmed/32493623 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ijscr.2020.01.032 |
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