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Congenital and inherited polycythemia.

作者信息

Kralovics R, Prchal J T

机构信息

University of Alabama at Birmingham, Division of Hematology/Oncology, 35294, USA.

出版信息

Curr Opin Pediatr. 2000 Feb;12(1):29-34. doi: 10.1097/00008480-200002000-00006.

DOI:10.1097/00008480-200002000-00006
PMID:10676771
Abstract

Absolute polycythemia is a condition with increased red blood cell mass. There are a number of primary and secondary polycythemic disorders leading to absolute polycythemia. Primary polycythemias are caused by a defect intrinsic to the erythroid progenitor cells. The best characterized primary polycythemia is the autosomal dominant primary familial and congenital polycythemia (PFCP). Familial or childhood occurrence of the myeloproliferative disorder polycythemia vera are also discussed, emphasizing the importance of distinction between polycythemia vera and PFCP. Congenital or familial secondary polycythemic conditions are characterized by increased red cell mass, which is caused by circulating serum factors, typically erythropoietin.

摘要

相似文献

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Basic sciences of the myeloproliferative diseases: pathogenic mechanisms of ET and PV.骨髓增殖性疾病的基础科学:原发性血小板增多症和真性红细胞增多症的发病机制
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Mouse model of congenital polycythemia: Homologous replacement of murine gene by mutant human erythropoietin receptor gene.
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