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Chronic haemolytic anaemia because of pyruvate kinase (PK) deficiency in a child heterozygous for haemoglobin S and no clinical features of sickle cell disease

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Bibliographic Details
Published in:	European journal of haematology 2010-01, Vol.84 (1), p.89-90
Main Authors:	Manco, Licínio, Vagace, José Manuel, Relvas, Luís, Rebelo, Umbelina, Bento, Celeste, Villegas, Ana, Letícia Ribeiro, Maria
Format:	Article
Language:	English
Subjects:	Adult Anemia, Hemolytic, Congenital Nonspherocytic - blood Anemia, Hemolytic, Congenital Nonspherocytic - complications Anemia, Hemolytic, Congenital Nonspherocytic - genetics beta-Globins - genetics Child Erythrocyte Indices Female Hemoglobin, Sickle - metabolism Heterozygote Humans Male Mutation, Missense Oxygen - blood Phenotype Point Mutation Pyruvate Kinase - deficiency Pyruvate Kinase - genetics Pyruvate Metabolism, Inborn Errors - blood Pyruvate Metabolism, Inborn Errors - enzymology Pyruvate Metabolism, Inborn Errors - genetics Sickle Cell Trait - blood Sickle Cell Trait - complications Sickle Cell Trait - genetics
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