Prevalence and management of iron overload in pyruvate kinase deficiency: report from the Pyruvate kinase deficiency natural history study

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

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Bibliographic Details
Main Authors: Beers, E.J. (Ward) van (Author) , Kunz, Joachim (Author)
Format: Article (Journal)
Language:English
Published: February 2019
In: Haematologica
Year: 2019, Volume: 104, Issue: 2, Pages: e51-e53
ISSN:1592-8721
DOI:10.3324/haematol.2018.196295
Online Access:Verlag, Volltext: http://dx.doi.org/10.3324/haematol.2018.196295
Verlag, Volltext: http://www.haematologica.org/content/104/2/e51
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Author Notes:Eduard J. van Beers, Stephanie van Straaten, D. Holmes Morton, Wilma Barcellini, Stefan W. Eber, Bertil Glader, Hassan M. Yaish, Satheesh Chonat, Janet L. Kwiatkowski, Jennifer A. Rothman, Mukta Sharma, Ellis J. Neufeld, Sujit Sheth, Jenny M. Despotovic, Nina Kollmar, Dagmar Pospíšilová, Christine M. Knoll, Kevin Kuo, Yves D. Pastore, Alexis A. Thompson, Peter E. Newburger, Yaddanapudi Ravindranath, Winfred C. Wang, Marcin W. Wlodarski, Heng Wang, Susanne Holzhauer, Vicky R. Breakey, Madeleine Verhovsek, Joachim Kunz, Melissa A. McNaull, Melissa J. Rose, Heather A. Bradeen, Kathryn Addonizio, Anran Li, Hasan Al-Sayegh, Wendy B. London, Rachael F. Grace
Description
Summary: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
Item Description:Gesehen am 28.02.2019
Physical Description:Online Resource
ISSN:1592-8721
DOI:10.3324/haematol.2018.196295