Rare combination of simple virilizing form of 21-hydroxylase deficiency, Graves’ disease and 47, XXX in a woman: A case report

Coexistence of congenital adrenal hyperplasia due to 21-hydroxylase deficiency, Graves’ disease and 47, XXX is rare. We report a case of a 25-year-old woman presented with masculine appearance, hirsutism and enlarged clitoris. Lab tests showed elevated serum 17 hydroxyprogesterone, testosterone, deh...

Descripción completa

Detalles Bibliográficos
Autores principales: Liang, Dong, Han, Minmin, Xu, Linxin, Ren, Yi, Zhang, Yi, Yin, Jianhong, Yang, Jing, Liu, Yunfeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
4300
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9622681/
https://www.ncbi.nlm.nih.gov/pubmed/36316845
http://dx.doi.org/10.1097/MD.0000000000031443

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9622681/
https://www.ncbi.nlm.nih.gov/pubmed/36316845
http://dx.doi.org/10.1097/MD.0000000000031443

Ejemplares similares