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

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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Bibliographic Details
Main Authors: Su Jin Lee, Je Eun Song, Sena Hwang, Ji-Yeon Lee, Hye-Sun Park, Seunghee Han, Yumie Rhee
Format: Article
Language:English
Published: Korean Endocrine Society 2015-09-01
Series:Endocrinology and Metabolism
Subjects:
Adrenocortical adenoma
Adrenal hyperplasia, congenital
Adrenal glands
Online Access:http://e-enm.org/Synapse/Data/PDFData/2008ENM/enm-30-408.pdf

Internet

http://e-enm.org/Synapse/Data/PDFData/2008ENM/enm-30-408.pdf

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