Rare Coexistence of Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency and Turner Syndrome: A Case Report and Brief Literature Review

The coexistence of congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency and Turner syndrome (TS) is rare. We report on a 6-year-old Portuguese girl with mosaic TS [45,XO(39)/47,XXX(21)] presenting with premature pubarche at the age of 5 years. Laboratory findings showed elevated 17-...

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Detalles Bibliográficos
Autores principales: Inácio, Isabel, Serra-Caetano, Joana, Cardoso, Rita, Dinis, Isabel, Mirante, Alice
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9976158/
https://www.ncbi.nlm.nih.gov/pubmed/34355878
http://dx.doi.org/10.4274/jcrpe.galenos.2021.2021.0174

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9976158/
https://www.ncbi.nlm.nih.gov/pubmed/34355878
http://dx.doi.org/10.4274/jcrpe.galenos.2021.2021.0174

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