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46,XX 性反转阴性的真两性畸形同胞。

46,XX SRY-negative true hermaphrodite siblings.

作者信息

Dorsey Faith Y, Hsieh Michael H, Roth David R

机构信息

Baylor College of Medicine, Houston, Texas 77030, USA.

出版信息

Urology. 2009 Mar;73(3):529-31. doi: 10.1016/j.urology.2008.09.050. Epub 2008 Nov 26.

Abstract

The sex-determining region on the Y chromosome (SRY) gene guides male sexual development. However, individuals with sex reversal syndrome (46,XX males and 46,XX true hermaphrodites) lack the SRY gene and yet can still develop testes. We present 2 siblings with XX true hermaphroditism. Most cases of sex reversal syndrome are sporadic; however, reports have been published of familial occurrence, suggesting that 46,XX maleness and 46,XX true hermaphroditism are actually different manifestations of the same disorder of gonadal development, likely an autosomal dominant mutation with variable penetrance or an X-linked mutation.

摘要

Y染色体性别决定区(SRY)基因引导男性性发育。然而,患有性反转综合征(46,XX男性和46,XX真两性畸形者)的个体缺乏SRY基因,但仍可发育出睾丸。我们报告了2例患有XX真两性畸形的同胞。大多数性反转综合征病例为散发性;然而,已有家族性发病的报道,这表明46,XX男性化和46,XX真两性畸形实际上是性腺发育同一疾病的不同表现形式,可能是一种具有可变外显率的常染色体显性突变或X连锁突变。

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