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...

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Detalles Bibliográficos
Autores principales: Lanciotti, Lucia, Cofini, Marta, Leonardi, Alberto, Bertozzi, Mirko, Penta, Laura, Esposito, Susanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6480640/
https://www.ncbi.nlm.nih.gov/pubmed/30970592
http://dx.doi.org/10.3390/ijerph16071268

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6480640/
https://www.ncbi.nlm.nih.gov/pubmed/30970592
http://dx.doi.org/10.3390/ijerph16071268

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