Fast Facts: Pyruvate Kinase Deficiency von Bertil Glader | ISBN 9783318072556

Fast Facts: Pyruvate Kinase Deficiency

von Bertil Glader, Wilma Barcellini und Rachael Grace
Mitwirkende
Autor / AutorinBertil Glader
Autor / AutorinWilma Barcellini
Autor / AutorinRachael Grace
Buchcover Fast Facts: Pyruvate Kinase Deficiency | Bertil Glader | EAN 9783318072556 | ISBN 3-318-07255-9 | ISBN 978-3-318-07255-6

Fast Facts: Pyruvate Kinase Deficiency

von Bertil Glader, Wilma Barcellini und Rachael Grace
Mitwirkende
Autor / AutorinBertil Glader
Autor / AutorinWilma Barcellini
Autor / AutorinRachael Grace
Pyruvate kinase (PK) deficiency is an inherited disease that affects red blood cells and manifests as hemolytic anemia. It is a lifelong condition, with symptoms that range from mild to severe. Despite an ever-growing understanding of its pathophysiology, etiology, and epidemiology, and an active research program, PK deficiency remains unfamiliar to many medical practitioners. PK deficiency is clinically heterogeneous, so healthcare professionals need to consider the possibility of this disorder in all patients with a congenital hemolytic anemia.