Prader-Willi syndrome and polygonosomal abnormalities in males:about a Prader-Willi/47,XYY patient

Ann Genet. 2001 Jan-Mar;44(1):1-3. doi: 10.1016/s0003-3995(01)01039-5.

Abstract

We herein report a male patient known as having a XYY karyotype. At the age of 26 years a Prader-Willi syndrome (PWS) was diagnosed. Before that time the whole symptomatology was ascribed to the XYY syndrome. This is the first reported association of PWS and polygonosomal abnormality in a male adult (whose height is above average).

Publication types

  • Case Reports
  • Review

MeSH terms

  • Adult
  • Body Height
  • Humans
  • Karyotyping
  • Male
  • Prader-Willi Syndrome / genetics*
  • X Chromosome
  • Y Chromosome