Untreated Congenital Adrenal Hyperplasia with 17-α Hydroxylase/17,20-Lyase Deficiency Presenting as Massive Adrenocortical Tumor

Congenital adrenal hyperplasia (CAH) with 17α-hydroxylase/17,20-lyase deficiency is usually characterized by hypertension and primary amenorrhea, sexual infantilism in women, and pseudohermaphroditism in men. hypertension, and sexual infantilism in women and pseudohermaphroditism in men. In rare cas...

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Detalles Bibliográficos
Autores principales: Lee, Su Jin, Song, Je Eun, Hwang, Sena, Lee, Ji-Yeon, Park, Hye-Sun, Han, Seunghee, Rhee, Yumie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Endocrine Society 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4595368/
https://www.ncbi.nlm.nih.gov/pubmed/26248854
http://dx.doi.org/10.3803/EnM.2015.30.3.408

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4595368/
https://www.ncbi.nlm.nih.gov/pubmed/26248854
http://dx.doi.org/10.3803/EnM.2015.30.3.408

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