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

• मुख्य लेखकों: Yunling Tian (लेखक), Lijie Hou (लेखक), Shulan Xiang (लेखक), Xuguang Tian (लेखक), Jinhui Xu (लेखक)
• स्वरूप: पुस्तक
• प्रकाशित: Taylor & Francis Group, 2023-12-01T00:00:00Z.
• विषय: article
• ऑनलाइन पहुंच: 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...