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

• Egile Nagusiak: Yunling Tian (Egilea), Lijie Hou (Egilea), Shulan Xiang (Egilea), Xuguang Tian (Egilea), Jinhui Xu (Egilea)
• Formatua: Liburua
• Argitaratua: Taylor & Francis Group, 2023-12-01T00:00:00Z.
• Gaiak: article
• Sarrera elektronikoa: 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...