| Literature DB >> 23284264 |
Rafael Fabiano Machado Rosa1, Rosana Cardoso Manique Rosa, Pedro Paulo Albino Dos Santos, Paulo Ricardo Gazzola Zen, Giorgio Adriano Paskulin.
Abstract
The 22q11.2 deletion syndrome (22q11DS) is a common genetic disease characterized by broad phenotypic variability. Despite the small number of studies describing hematological alterations in individuals with 22q11DS, it appears that these abnormalities are more frequent than previously imagined. Thus, the objective of our study was to report on a patient with 22q11DS presenting thrombocytopenia and large platelets and to review the literature. The patient, a 13-year-old boy, was originally evaluated due to craniofacial dysmorphia and speech delay. He also had a history of behavioral changes, neuropsychomotor delay and recurrent otitis/sinusitis. The identification of a 22q11.2 microdeletion by fluorescent in situ hybridization diagnosed the syndrome. Despite his hematological alterations, he only had a history of epistaxis and bruising of the upper and lower limbs. Assessments of the prothrombin time, thrombin time, partial thromboplastin time, bleeding time, fibrinogen levels and platelet aggregation (including the ristocetin induced platelet aggregation test) were all normal. Hematological alterations observed in 22q11DS are directly related to the genetic disorder itself (especially in respect to deletion of the GPIb gene) and secondary to some clinical findings, such as immunodeficiency. Macrothrombocytopenia is increasingly being considered a feature of the broad spectrum of 22q11DS and may potentially be a clinical marker for the syndrome.Entities:
Keywords: Bernard-Soulier syndrome; Blood platelets; Chromosomes, Human, Pair 22; DiGeorge syndrome; In situ hybridization; Thrombocytopenia
Year: 2011 PMID: 23284264 PMCID: PMC3520641 DOI: 10.5581/1516-8484.20110037
Source DB: PubMed Journal: Rev Bras Hematol Hemoter ISSN: 1516-8484