先天性肾上腺增生
医学
内分泌学
内科学
病理生理学
增生
雄激素
甾体11β-羟化酶
雄激素过量
分泌物
21羟化酶
类固醇
激素
肥胖
胰岛素抵抗
多囊卵巢
作者
Cem Demirci,Selma F. Witchel
标识
DOI:10.1111/j.1529-8019.2008.00216.x
摘要
The congenital adrenal hyperplasias are a group of autosomal recessive disorders associated with impaired steroidogenesis. Several types of the congenital adrenal hyperplasias are associated with decreased cortisol production and excessive adrenal sex steroid secretion. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency is the most common and prototypic example of this group of disorders. Herein, we review the clinical features, pathophysiology, molecular genetics, and treatment of 21-hydroxylase deficiency. There is also a brief discussion of other steroidogenic enzyme defects that are associated with clinical features due to excessive androgen secretion.
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