Pyruvate kinase (PK) deficiency is the most common red cell glycolytic enzyme defect causing hereditary non-spherocytic hemolytic anemia. Current treatments are mainly supportive and include red cell transfusions and splenectomy.[1][1] Regular red cell transfusions are known to result in iron
Prevalence and management of iron overload in pyruvate kinase deficiency: report from the Pyruvate Kinase Deficiency Natural History Study
E. V. van Beers,S. van Straaten,D. Morton,W. Barcellini,S. Eber,B. Glader,H. Yaish,S. Chonat,J. Kwiatkowski,J. Rothman,Mukta Sharma,E. Neufeld,S. Sheth,J. Despotovic,N. Kollmar,D. Pospíšilová,C. Knoll,K. Kuo,Y. Pastore,A. Thompson,P. Newburger,Y. Ravindranath,Winfred C. Wang,M. Wlodarski,Heng Wang,S. Holzhauer,V. Breakey,M. Verhovsek,J. Kunz,Melissa A. McNaull,M. Rose,Heather A. Bradeen,K. Addonizio,Anran Li,Hasan Al-Sayegh,W. London,R. Grace
Published 2018 in Haematologica
ABSTRACT
PUBLICATION RECORD
- Publication year
2018
- Venue
Haematologica
- Publication date
2018-09-13
- Fields of study
Medicine
- Identifiers
- External record
- Source metadata
Semantic Scholar, PubMed
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