家族性莱迪希细胞发育不全作为男性假两性畸形的一个病因
Familial Leydig cell hypoplasia as a cause of male pseudohermaphroditism.
作者信息
el-Awady M K, Temtamy S A, Salam M A, Gad Y Z
出版信息
Hum Hered. 1987;37(1):36-40. doi: 10.1159/000153675.
PMID:3557461
Abstract
A case of familial Leydig cell hypoplasia as a cause of male pseudohermaphroditism is described in two 46,XY female sibs. Biochemical and histologic evidence for such diagnosis is presented.
摘要
本文描述了一例家族性莱迪希细胞发育不全导致男性假两性畸形的病例，患者为两名46,XY核型的女性同胞。文中给出了支持该诊断的生化和组织学证据。
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