Thrombocytopenia in patients with 22q11.2 deletion syndrome and its association with glycoprotein Ib-beta

Genet Med. 2003 Mar-Apr;5(2):113-9. doi: 10.1097/01.GIM.0000056828.03164.30.

Abstract

Purpose: To elucidate whether thrombocytopenia in 22q11.2 deletion syndrome patients is associated with the hemizygosity of glycoprotein Ib-beta and to clarify the correlation of phenotype and genotype of this gene in 22q11.2 deletion syndrome patients with thrombocytopenia.

Methods: Platelet number, mean platelet volume, platelet agglutination, and the protein level of glycoprotein Ib-beta were measured in 22q11.2 deletion syndrome patients and controls. Phenotypes other than that of thrombocytopenia were also analyzed in these patients.

Results: The 22q11.2 deletion syndrome patients with thrombocytopenia had a larger mean platelet volume, lower agglutination to ristocetin, and lower protein level of glycoprotein Ib-beta than control patients. The 22q11.2 deletion syndrome patients with thrombocytopenia showed an increased risk of developing schizophrenia.

Conclusions: Thrombocytopenia in 22q11.2 deletion syndrome patients is associated with decreased expression of glycoprotein Ib-beta because of the hemizygosity. 22q11.2 deletion syndrome patients with thrombocytopenia require total management, especially for schizophrenia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Blotting, Western
  • Child
  • Child, Preschool
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 22*
  • Female
  • Humans
  • In Situ Hybridization, Fluorescence
  • Male
  • Phenotype
  • Platelet Count
  • Platelet Glycoprotein GPIb-IX Complex / genetics*
  • Sequence Analysis, DNA
  • Thrombocytopenia / blood
  • Thrombocytopenia / genetics*

Substances

  • Platelet Glycoprotein GPIb-IX Complex