摘要
先天性肾上腺皮质增生症(congenital adrenal hyperplasia,CAH)是一组常染色体隐性遗传疾病,由肾上腺皮质激素合成途径中酶的缺陷所引起。最常见的酶缺陷类型为21-羟化酶缺乏(21-hydroxylase deficiency,21-OHD),占酶缺陷类型的90%,根据酶的缺陷程度又分为经典型及非经典型两种临床类型,儿童中主要为经典型。
作者
陈欣欣(综述)
朱岷(审校)
Chen Xinxin Zhu Min(Children' s Hospital of Chongqing Medical University, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Pediatrics, China International Science and Technology Cooperation Base of Child Development and Critical Disorders, Chongqing Key Laboratory of Pediatrics, Chongqing 400014, China)
出处
《儿科药学杂志》
CAS
2017年第10期60-63,共4页
Journal of Pediatric Pharmacy