Dyserythropoiesis in a child with pyruvate kinase deficiency and coexistent unilateral multicystic dysplastic kidney

Pediatric Blood and Cancer

Volumn 61, Issue 8, 2014, Pages 1463-1465

  Haija, Marwa Abu El ^a   Qian, You Wen ^b   Muthukumar, Akila ^a  

^a UNIVERSITY OF TEXAS MEDICAL BRANCH   (United States)

^b University of Texas Medical Branch School of Medicine   (United States)

Author keywords

Dyserythropoiesis; Hemolytic anemia; Multicystic dysplastic kidney; Pyruvate kinase deficiency

Indexed keywords

HEMOGLOBIN; OXYGEN; PYRUVATE KINASE;

ANEMIA; APGAR SCORE; ARTICLE; BLOOD CELL COUNT; BONE MARROW BIOPSY; CASE REPORT; CHILDHOOD DISEASE; CHROMATIN; CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE 1; DYSERYTHROPOIESIS; ECHOCARDIOGRAPHY; ELECTRON MICROSCOPY; ENZYME ACTIVITY; ENZYME DEFICIENCY; ERYTHROBLAST; ERYTHROCYTE; ERYTHROCYTE TRANSFUSION; ERYTHROPOIESIS; EXON; FETUS ECHOGRAPHY; GENE; GENE MUTATION; GENE SEQUENCE; HEART ATRIUM SEPTUM DEFECT; HEMOGLOBIN BLOOD LEVEL; HETEROZYGOTE; HUMAN; INFANT; IRON DEFICIENCY; MALE; MULTICYSTIC DYSPLASTIC KIDNEY; NEWBORN INTENSIVE CARE; NUCLEAR MAGNETIC RESONANCE IMAGING; OLIGOHYDRAMNIOS; OXYGEN CONSUMPTION; PERICARDIAL EFFUSION; PHYSICAL EXAMINATION; PKLR GENE; PRIORITY JOURNAL; PUERPERIUM; RESUSCITATION; RETICULOCYTE; RETICULOCYTE COUNT; SMEAR; STIMULATION; SYSTOLIC HEART MURMUR; THIRD TRIMESTER PREGNANCY; THROMBOCYTE; THROMBOCYTOPENIA;

DYSERYTHROPOIESIS; HEMOLYTIC ANEMIA; MULTICYSTIC DYSPLASTIC KIDNEY; PYRUVATE KINASE DEFICIENCY;

ADULT; ANEMIA, DYSERYTHROPOIETIC, CONGENITAL; ANEMIA, HEMOLYTIC, CONGENITAL NONSPHEROCYTIC; FEMALE; HUMANS; INFANT, NEWBORN; MALE; MULTICYSTIC DYSPLASTIC KIDNEY; MUTATION; PYRUVATE KINASE; PYRUVATE METABOLISM, INBORN ERRORS;

EID: 84901990074     PISSN: 15455009     EISSN: 15455017     Source Type: Journal    
DOI: 10.1002/pbc.24953     Document Type: Article

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