Primary familial and congenital polycythemia; The forgotten entity

Primary familial and congenital polycythemia; The forgotten entity

Primary familial and congenital polycythemia (PFCP) is a rare autosomal dominant disorder caused by hypersensitivity of erythropoietin receptor of erythroid progenitors leading to increased rate of erythropoiesis at any given serum erythropoietin level. The hallmark of this disorder is isolated eryt...

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Bibliographic Details
Main Author: Mansour S Aljabry
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2018-01-01
Series:Journal of Applied Hematology
Subjects:
Polycythemia
Polycythemia Vera
primary familial and congenital polycythemia
Online Access:http://www.jahjournal.org/article.asp?issn=1658-5127;year=2018;volume=9;issue=2;spage=39;epage=44;aulast=Aljabry

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http://www.jahjournal.org/article.asp?issn=1658-5127;year=2018;volume=9;issue=2;spage=39;epage=44;aulast=Aljabry

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