A girl with the Prader-Willi syndrome and Robertsonian translocation 45,XX,t(14;15)(p11;q11) which was present in three normal family members

Hum Genet. 1980;55(2):271-3. doi: 10.1007/BF00291777.

Abstract

A 21-year-old girl with classical Prader-Willi Syndrome was found to have a 14;15 Robertsonian translocation--45,XX,t(14;15)(p11;q11). This type of Robertsonian translocation was not found in any patient from 8 surveys covering 6144 patients with mental retardation. Chromosome 15 has been involved in translocations in patients with the Prader-Willi Syndrome with greater than expected frequency. This is the first report of a 14;15 translocation and the Prader-Willi Syndrome. The same balanced translocation was present in the patient's mother and 2 normal siblings. Future genetic counselling for these 2 siblings will be difficult.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Chromosomes, Human, 13-15 / ultrastructure*
  • Female
  • Genetic Counseling
  • Humans
  • Male
  • Pedigree
  • Prader-Willi Syndrome / genetics*
  • Translocation, Genetic*