Importance of jak-2 gene mutation in the diagnosis of polycythemia vera: a case report and review of the literature
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Case Reports
P: 35-38
March 2010

Importance of jak-2 gene mutation in the diagnosis of polycythemia vera: a case report and review of the literature

Med J Bakirkoy 2010;6(1):35-38
1. Haydarpaşa Numune Eğitim ve Araştırma Hastanesi 4. Dahiliye Kliniği, İstanbul
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Received Date: 11.05.2009
Accepted Date: 01.09.2009
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ABSTRACT

Polycythemia vera is an acquired myeloproliferative disorder that causes overproduction of all three hematopoietic cell lines, most prominently the red blood cells. The most common of the chronic myeloproliferative disorders, polycythemia vera occurs in about 0,5-2 per 100,000 persons. A slight overall male predominance has been observed, but females predominate within the reproductive age range. In this case report, We aimed to emphasize that cytogenetic analysis recently is important in the diagnosis of polycythemia vera.

Keywords:
Polycythemia vera, Jak-2 gene mutation, gastrointestinal bleeding