Characterization of the Severe Phenotype of Pyruvate Kinase Deficiency

Background: Pyruvate kinase deficiency (PKD) is the most common cause of chronic hereditary non-spherocytic hemolytic anemia. The spectrum of disease in PKD is broad, ranging from an incidentally discovered mild anemia to a severe transfusion-dependent anemia. Splenectomy partially ameliorates the a...

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Bibliographic Details

Published in:	Blood Vol. 134; no. Supplement_1; p. 949
Main Authors:	Al-Samkari, Hanny, van Beers, Eduard J., Morton, D Holmes, Barcellini, Wilma, Eber, Stefan W., Glader, Bertil, Yaish, Hassan M., Chonat, Satheesh, Kuo, Kevin H.M., Kollmar, Nina, Despotovic, Jenny M., Pospisilova, Dagmar, Knoll, Christine M., Kwiatkowski, Janet L., Pastore, Yves D., Thompson, Alexis A., Wlodarski, Marcin W., Ravindranath, Yaddanapudi, Rothman, Jennifer A., Wang, Heng, Holzhauer, Suzanne, Breakey, Vicky R., Verhovsek, Madeleine M., Kunz, Joachim B., Sheth, Sujit, Sharma, Mukta, Rose, Melissa J., Bradeen, Heather, McNaull, Melissa A., Addonizio, Kathryn, Al-Sayegh, Hasan, London, Wendy B., Grace, Rachael F.
Format:	Journal Article
Language:	English
Published:	Elsevier Inc 13-11-2019
Online Access:	Get full text
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