Severe impact of late diagnosis of congenital adrenal hyperplasia on gender identity, sexual orientation and function: case report and review of the literature

Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency (21-OHD) represents the most frequent form of CAH and of 46, XX disorder of sex development in female newborns. In the majority of cases, particularly in developed countries, female patients suffering from the classic forms of CAH...

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Detalles Bibliográficos
Autores principales: Simeoli, Chiara, de Angelis, Cristina, Delli Veneri, Alessandra, Menafra, Davide, Di Paola, Nicola, Pivonello, Claudia, Di Somma, Carolina, Valerio, Paolo, Melis, Daniela, Alviggi, Carlo, Colao, Annamaria, Pivonello, Rosario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9661730/
https://www.ncbi.nlm.nih.gov/pubmed/36386789
http://dx.doi.org/10.3389/fgene.2022.902844

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