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真两性畸形中的遗传异质性。两例报告。

Genetic heterogeneity in true hermaphrodites. A report of two cases.

作者信息

Kucheria K, Mohapatra I, Taneja N, Gupta D K, Ammini A C

机构信息

Department of Anatomy, All India Institute of Medical Sciences, New Delhi.

出版信息

J Reprod Med. 1994 Jul;39(7):550-2.

PMID:7966049
Abstract

True hermaphrodites are identified from the presence of ambiguous genitalia with both ovarian and testicular tissue. Two cases presented below had a 46,XX chromosome pattern, cryptorchidism and undescended testes. Both cases showed an absence of secondary sexual characteristics and presence of bilateral breasts and a uterus. The gonads in case 1 were an ovotestis and testis (left side) and in case 2 were an ovary and testis (right side). Case 1 was analyzed for a sex-determining region on the Y chromosome (SRY) and was negative. Phenotypic, gonadal and molecular studies suggest that 46,XX true hermaphroditism is a genetically heterogeneous condition.

摘要

真性两性畸形是通过存在具有卵巢和睾丸组织的两性生殖器来确定的。以下介绍的两个病例具有46,XX染色体模式、隐睾症和睾丸未降。两个病例均表现为缺乏第二性征,双侧乳房和子宫存在。病例1的性腺为卵睾和睾丸(左侧),病例2的性腺为卵巢和睾丸(右侧)。对病例1进行了Y染色体性别决定区(SRY)分析,结果为阴性。表型、性腺和分子研究表明,46,XX真性两性畸形是一种基因异质性疾病。

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