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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Vydáno v:Endocrinol Metab (Seoul)
Hlavní autoři: Lee, Su Jin, Song, Je Eun, Hwang, Sena, Lee, Ji-Yeon, Park, Hye-Sun, Han, Seunghee, Rhee, Yumie
Médium: Artigo
Jazyk:Inglês
Vydáno: Korean Endocrine Society 2015
Témata:
Case Report
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4595368/
https://ncbi.nlm.nih.gov/pubmed/26248854
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3803/EnM.2015.30.3.408
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