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Erythrocyte pyruvate kinase deficiency. A case of severe congenital hemolytic anemia.
Mo Med ; 86(2): 92-4, 1989 Feb.
Article in En | MEDLINE | ID: mdl-2761512
Although it occurs rarely, erythrocyte pyruvate kinase deficiency is a cause of neonatal jaundice and anemia across many ethnic and geographic groups. In this report of a Missouri case, an infant with this condition was also found to have Pelger-Huet leukocyte anomaly.
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Database: MEDLINE Main subject: Pelger-Huet Anomaly / Pyruvate Kinase / Pyruvate Metabolism, Inborn Errors / Erythrocytes / Anemia, Hemolytic, Congenital Type of study: Diagnostic_studies Limits: Female / Humans / Newborn Language: En Journal: Mo Med Year: 1989 Type: Article
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Database: MEDLINE Main subject: Pelger-Huet Anomaly / Pyruvate Kinase / Pyruvate Metabolism, Inborn Errors / Erythrocytes / Anemia, Hemolytic, Congenital Type of study: Diagnostic_studies Limits: Female / Humans / Newborn Language: En Journal: Mo Med Year: 1989 Type: Article