A case of double trisomy in a liveborn infant: 48, XXY, + 13

John B. Mailhes, Charleen M. Moore, Juan J. Gershanik

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Abstract

Ambiguous genitalia, microcephaly, microphthalmia, hypotelorisrn, single choanal opening, low‐set ears, simian creases, Tetralogy of Fallot, bilateral hydronephrosis, and absence of the left ureter characterized an infant that died 1 hour postpartum with the karyotype 48,XXY,+13.

Original languageEnglish (US)
Pages (from-to)147-150
Number of pages4
JournalClinical Genetics
Volume11
Issue number2
DOIs
StatePublished - Feb 1977

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ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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