Brief clinical report: Dysgenetic male pseudohermaphroditism in 45,X/46,Xdel(Y)(q11.1) mosaic infant

A. R. Gaba; D. L. Van Dyke; L. Weiss

doi:10.1002/ajmg.1320260306

Brief clinical report: Dysgenetic male pseudohermaphroditism in 45,X/46,Xdel(Y)(q11.1) mosaic infant

A. R. Gaba, D. L. Van Dyke, L. Weiss

Laboratory Medicine and Pathology

Research output: Contribution to journal › Article › peer-review

Abstract

We describe an infant with dysgenetic male pseudohermaphroditism and the karyotype 45,X/46,X,del(Y)(q11.1). Histologic examination of the resected gonads showed cortical dysplasia indicative of incipient gonadoblastoma.

Original language	English (US)
Pages (from-to)	545-549
Number of pages	5
Journal	American journal of medical genetics
Volume	26
Issue number	3
DOIs	https://doi.org/10.1002/ajmg.1320260306
State	Published - 1987

ASJC Scopus subject areas

Genetics
Genetics(clinical)

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abstract = "We describe an infant with dysgenetic male pseudohermaphroditism and the karyotype 45,X/46,X,del(Y)(q11.1). Histologic examination of the resected gonads showed cortical dysplasia indicative of incipient gonadoblastoma.",

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Brief clinical report: Dysgenetic male pseudohermaphroditism in 45,X/46,Xdel(Y)(q11.1) mosaic infant

Abstract

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