1例46,XX/47,XXY卵睾型性发育异常多学科诊治病例报告  

Multi-disciplinary Treatment of a Patient with 46,XX/47,XXY Ovo-testicular Disorder of Sex Development:a case report

作　　者：王丹[1] 范新钊 何美男 蒲美岑 曹瑛[1] Wang Dan;Fan Xinzhao;He Meinan;Pu Meichen;Cao Ying(Department of Endocrinology and Metabolism,Nanfang Hospital,Southern Medical University,Guangzhou 510515,China;Department of Endocrinology and Metabolism,Nanfang Hospital Zengcheng Branch,Southern Medical University,Guangzhou 511338,China)

机构地区：[1]南方医科大学南方医院内分泌代谢科,广州510515 [2]南方医科大学南方医院增城分院内分泌代谢科,广州511338

出　　处：《国际内分泌代谢杂志》2024年第3期212-216,共5页International Journal of Endocrinology and Metabolism

摘　　要：卵睾型性发育异常(ovo-testicular disorders of sex development,OT-DSD)是指同一个体内具有卵巢和睾丸两种性腺组织,且两种性腺都有一定程度功能[1]。发病率相对较低,约为新生儿的1/10万[2],占所有DSD病例的3%~10%[3-5]。本文报道1例染色体核型为罕见46,XX/47,XXY OT-DSD的儿童患者多学科诊治经过。

关 键 词：多学科诊治 卵睾型性发育异常 病例报告 儿童患者 染色体核型 DSD 新生儿 

分 类 号：R588[医药卫生—内分泌]