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

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.
Taichi Kato 1 Kazuki Kosaka Misa Kimura Shin-Ichiro Imamura Osamu Yamada Kazumasa Iwai Masahiko Ando Kunitaka Joh-o Kenji Kuroe Akira Ohtake Atsuyoshi Takao Kazuo Momma Rumiko Matsuoka
Affiliations

Affiliation

  • 1 Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
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.

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