Diagnosis and clinical course of congenital dyserythropoietic anaemia type 1 in a 12-year-old girl

European Journal of Pediatrics

Volumn 160, Issue 2, 2001, Pages 139-140

  Rössler, Jochen ^a   Heimpel, Hermann ^b   Havers, Werner ^a  

^a UNIVERSITY OF DUISBURG ESSEN   (Germany)

^b UNIVERSITY OF ULM   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CYANOCOBALAMIN; IRON;

ARTICLE; BLOOD SMEAR; CASE REPORT; EARLY DIAGNOSIS; ERYTHROCYTE TRANSFUSION; ERYTHROPOIESIS; FEMALE; HEPATOSPLENOMEGALY; HEREDITARY HEMOLYTIC ANEMIA; HUMAN; HYPERBILIRUBINEMIA; IRON THERAPY; PHOTOTHERAPY; PRIORITY JOURNAL; SCHOOL CHILD;

ANEMIA, DYSERYTHROPOIETIC, CONGENITAL; CHILD; FEMALE; HUMANS;

EID: 0035105671     PISSN: 03406199     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004310000677     Document Type: Article

References (6)

1. Congenital dyserythropoietic anemia with karyorrhexis and multinuclearity of erythroplasts
2. Neonatal manifestations of congenital dyserythropoietic anemia type 1
3. Clinical features and studies of erythropoiesis in Israeli Bedouins with congenital dyserythropoietic anemia type 1
4. No response to recombinant human erythropoietin therapy in patients with congenital dyserythropoietic anemia type 1
5. Congenital dyserythropoiesis type 1 and alpha-interferon therapy
6. Dyserythropoiesis and congenital dyserythropoietic anaemias