17α－羟化酶缺陷症的诊断和治疗──13例临床经验  

DIAGNOSIS AND MANAGEMENT OF 17-HYDROXYLASE DEFICIENCY:A SUMMARY OF 13 CASES

作　　者：陆召磷 宋文英[1] 张平 郭爱丽[1] 张洁萍[1] 

机构地区：[1]北京协和医院内分泌科

出　　处：《中华内分泌代谢杂志》1994年第4期195-197,共3页Chinese Journal of Endocrinology and Metabolism

摘　　要：在先天性肾上腺皮质增生症（ＣＡＨ）中，１７α－羟化酶缺陷症（１７α－ＨＤ）很少见。截至１９９１年，在国外文献中只收集到１２０例，至今国内文献能查到的仅有８例报告。作者总结了自１９７８年至１９９２年期间收治的１３例１７α的临床资料，对诊断和治疗进行了讨论。Among the congenital adrenal hyperplasia(CAH),17-Hydroxylase deficiency(17-HD)is rare. Only about 120 cases were collect-ed in the foreign literatures by 1991, and there were only 8 cases reported in Chinese journals till now.We summarized the experi-ences of diagnosis and management of 13 cases of 17-HD accumulated in this hospital from 1978 to 1992.

关 键 词：羟化酶缺陷症 肾上腺皮质增生 诊断 治疗 

分 类 号：R586.9[医药卫生—内分泌] R362[医药卫生—内科学]