Uniparental paternal disomy in Angelman's syndrome

Lancet. 1991 Mar 23;337(8743):694-7. doi: 10.1016/0140-6736(91)90278-w.


Angelman's syndrome and Prader-Willi syndrome are both causes of mental retardation with recognisable, but quite different, clinical phenotypes. Both are associated with deletions of chromosome 15q11-13, of maternal origin in Angelman's and paternal in Prader-Willi. Prader-Willi can arise by inheritance of two chromosomes 15 from the mother and none from the father (uniparental maternal disomy). In 2 patients with Angelman's syndrome we found evidence of uniparental paternal disomy. The phenotypic effects of maternal and paternal disomy of chromosome 15 are very different and inheritance of two normal 15s from one parent does not lead to normal development--strong evidence in man for genomic imprinting, in which the same gene has different effects dependent upon its parental origin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Child
  • Child, Preschool
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 15*
  • DNA Probes
  • Electroencephalography
  • Face / abnormalities*
  • Fathers*
  • Female
  • Genomic Library*
  • Humans
  • Intellectual Disability / genetics*
  • Intellectual Disability / physiopathology
  • Karyotyping
  • Male
  • Mothers*
  • Phenotype
  • Recurrence
  • Syndrome


  • DNA Probes