当前位置:
X-MOL 学术
›
Hum. Reprod. Update
›
论文详情
Our official English website, www.x-mol.net, welcomes your
feedback! (Note: you will need to create a separate account there.)
Non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency revisited: an update with a special focus on adolescent and adult women
Human Reproduction Update ( IF 14.8 ) Pub Date : 2017-06-05 , DOI: 10.1093/humupd/dmx014 Enrico Carmina , Didier Dewailly , Héctor F. Escobar-Morreale , Fahrettin Kelestimur , Carlos Moran , Sharon Oberfield , Selma F. Witchel , Ricardo Azziz
Human Reproduction Update ( IF 14.8 ) Pub Date : 2017-06-05 , DOI: 10.1093/humupd/dmx014 Enrico Carmina , Didier Dewailly , Héctor F. Escobar-Morreale , Fahrettin Kelestimur , Carlos Moran , Sharon Oberfield , Selma F. Witchel , Ricardo Azziz
Non-classic congenital hyperplasia (NCAH) due to 21-hydroxylase deficiency is a common autosomal recessive disorder characterized by androgen excess.
中文翻译:
再次探讨由于21-羟化酶缺乏症引起的非经典性先天性肾上腺增生:这一更新特别关注青少年和成年女性
由21-羟化酶缺乏症引起的非经典性先天性增生(NCAH)是一种常见的常染色体隐性遗传疾病,其特征是雄激素过多。
更新日期:2017-06-05
中文翻译:
再次探讨由于21-羟化酶缺乏症引起的非经典性先天性肾上腺增生:这一更新特别关注青少年和成年女性
由21-羟化酶缺乏症引起的非经典性先天性增生(NCAH)是一种常见的常染色体隐性遗传疾病,其特征是雄激素过多。