The phenotype of a 45,X male with a Y/18 translocation

Giorgio Gimelli, Roberta Cinti, Paolo Varone, Arturo Naselli, Eliana Di Battista, Annalisa Pezzolo

Research output: Contribution to journalArticle

Abstract

In this report, we describe a male infant with a 45,X karyotype; the entire short arm and the centromere of the Y chromosome were translocated onto the short arm of chromosome 18, resulting in an unbalanced dicentric chromosome. Breakpoints were identified by in situ fluorescence hybridization (FISH) on the proximal Yq11 and 18p11.2. Both Y and 18 centromeric alphoid sequences were identified on the derived 18 chromosome. Clinical features were compatible with 18p- syndrome and no Turner stigmata were present in our propositus. Short stature was likely to be related to the deletion of 18p and/or Yq, where a gene involved in stature determination has been located proximal to a gene involved in spermatogenesis (AZF).

Original languageEnglish
Pages (from-to)37-41
Number of pages5
JournalClinical Genetics
Volume49
Issue number1
Publication statusPublished - Jan 1996

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Keywords

  • Chromosome 18
  • Chromosome-Y fluorescence in situ hybridization
  • Unbalanced translocation
  • XO male

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Gimelli, G., Cinti, R., Varone, P., Naselli, A., Di Battista, E., & Pezzolo, A. (1996). The phenotype of a 45,X male with a Y/18 translocation. Clinical Genetics, 49(1), 37-41.