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Different Clinical Presentations and Management in Complete Androgen Insensitivity Syndrome (CAIS)
Complete androgen insensitivity syndrome (CAIS) is an X-linked recessive genetic disorder resulting from maternally inherited or de novo mutations involving the androgen receptor gene, situated in the Xq11-q12 region. The diagnosis is based on the presence of female external genitalia in a 46, XY hu...
Gardado en:
| Publicado en: | Int J Environ Res Public Health |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
MDPI
2019
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6480640/ https://ncbi.nlm.nih.gov/pubmed/30970592 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijerph16071268 |
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