Thrombocytopenia in patients with chromosome 22q11.2 deletion syndrome

J Pediatr. 2003 Aug;143(2):277-8. doi: 10.1067/S0022-3476(03)00248-8.

Abstract

Thrombocytopenia is a common finding in patients with chromosome 22q11.2 deletion syndrome. Patients with chromosome 22q11.2 deletion syndrome (n=112) were analyzed along with 57 age-matched controls. Even after the exclusion of patients with idiopathic thrombocytopenia purpura, the mean platelet count was approximately 70% of the control population.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Child
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 22*
  • DiGeorge Syndrome / genetics*
  • Humans
  • Retrospective Studies
  • Syndrome
  • Thrombocytopenia / genetics*