A monozygotic twin pair with highly discordant Gaucher phenotypes

Blood Cells Mol Dis. 2011 Jan 15;46(1):39-41. doi: 10.1016/j.bcmd.2010.10.007. Epub 2010 Nov 5.

Abstract

We describe monozygotic twin sisters, born to consanguineous Moroccan parents, who are highly discordant for the manifestations of Gaucher disease. Both carry Gaucher genotype N188S/N188S. One has severe visceral involvement, epilepsy, and a cerebellar syndrome. Her twin does not manifest any symptoms or signs of Gaucher disease but suffers from type 1 diabetes mellitus. The concurrence of a mild Gaucher mutation with a severe phenotype, as well as the occurrence of highly discordant phenotypes in a pair of monozygotic twins, is discussed.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Adult
  • Cerebellar Diseases / etiology*
  • Diabetes Mellitus, Type 1 / complications*
  • Diseases in Twins*
  • Female
  • Gaucher Disease* / complications
  • Gaucher Disease* / diagnosis
  • Gaucher Disease* / genetics
  • Gaucher Disease* / pathology
  • Genotype
  • Glucosylceramidase / blood
  • Humans
  • Morocco
  • Mutation
  • Phenotype*
  • Twins, Monozygotic* / genetics
  • Young Adult

Substances

  • Glucosylceramidase