1987•American Journal of Medical GeneticsRequires access

Dysgenetic male pseudohermaphroditism in a 45,X/46,X,del(Y)(q11.1) mosaic infant

Arthur R. Gaba, Daniel L. Van Dyke, Laster Weiss, John M. Opitz, James F. Reynolds

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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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What this paper is about

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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Available 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.

Key concepts: Gonadoblastoma, Male pseudohermaphroditism, Pseudohermaphroditism, Karyotype, Dysplasia, Medicine, Biology, Gynecology

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Dysgenetic male pseudohermaphroditism in a 45,X/46,X,del(Y)(q11.1) mosaic infant — Research Paper | ScholarLens