Congenital adrenal hyperplasia disorder due to 17 α-hydroxylase deficiency: a case report

• Asıl Yazarlar: Yunling Tian (Yazar), Lijie Hou (Yazar), Shulan Xiang (Yazar), Xuguang Tian (Yazar), Jinhui Xu (Yazar)
• Materyal Türü: Kitap
• Baskı/Yayın Bilgisi: Taylor & Francis Group, 2023-12-01T00:00:00Z.
• Konular: article
• Online Erişim: Connect to this object online.

Congenital adrenal hyperplasia (CAH) is an autosomal recessive disorder with a related enzyme deficiency involved in the adrenal corticosteroid synthesis pathway due to genetic mutations. 17α-hydroxylase deficiency(17α-OHD) is a rare form of CAH. Herein, we reported clinical data on diagnosis and tr...