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

Research output: Contribution to journalArticle

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 languageEnglish (US)
Pages (from-to)545-549
Number of pages5
JournalAmerican journal of medical genetics
Volume26
Issue number3
DOIs
StatePublished - Jan 1 1987

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Fingerprint Dive into the research topics of 'Brief clinical report: Dysgenetic male pseudohermaphroditism in 45,X/46,Xdel(Y)(q11.1) mosaic infant'. Together they form a unique fingerprint.

  • Cite this