Congenital dyserythropoietic anaemia: Report of three cases

Journal of Paediatrics and Child Health

Volumn 32, Issue 2, 1996, Pages 191-193

  Ariffin, W A ^a   Karnaneedi, S ^b   Choo, K E ^c   Normah, J ^d  

^a HOSPITAL KUALA LUMPUR   (Malaysia)

^b Hospital Kangar   (Malaysia)

^c General Hospital Kota Bharu   (Malaysia)

^d HOSPITAL UNIVERSITI SAINS MALAYSIA   (Malaysia)

Author keywords

Blood transfusions; Bone marrow transplantation; Congenital dyserythropoietic anaemia

Indexed keywords

ANEMIA; ARTICLE; BLOOD TRANSFUSION; BONE MARROW TRANSPLANTATION; CASE REPORT; ERYTHROPOIESIS; FEMALE; HUMAN; INFANT; MALE; NEWBORN; ONSET AGE; PRESCHOOL CHILD; PRIORITY JOURNAL; SIBLING;

EID: 0029931058     PISSN: 10344810     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1440-1754.1996.tb00921.x     Document Type: Article

References (12)

1. Verwilghen RL, Lewis SM, Dacie JV, Crookston JH, Crookston MC. HEMPAS: Congenital dyserythropoietic anaemia (Type II). Q. J. Med. 1973; 42: 257-8.
2. Heimpel H, Wendt F. Congenital dyserythropoietic anaemia with karyorrhexis and multinuclearity of erythroblasts. Helv. Med. Acta 1968; 34: 103-5.
3. Villegas A, Gonzales L, Furio V et al. Congenital dyserythropoietic anaemia type III with unbalanced globin chain synthesis (Letter). Eur. J. Haematol. 1994; 52: 251-3.
4. Beutler E, Valentine WN. The congenital dyserythropoietic anemias. In Willians WJ, Beutler E, Erslev AJ, Lichtman MA, eds. Hematology 4th edn (International edn) McGraw-Hill, 1991; 448-52.
5. Mori PG, Favareto F, Schenone A et al. Congenital dyserythropoietic anaemia type I: report of a pair of siblings. Acta Hematol. 1986; 75: 219-23.
6. Jandl JH. Congenital dyserythropoietic anaemia. In Jandl JH, ed. Blood: Textbook of Haematology. Little, Brown, Boston. 1987; 133-4.
7. Alter BP, Young NS. The bone marrow failure syndromes. In Nathan DG, Oski FA, eds. Haematology of Infancy and Childhood, 4th edn. WB Saunders, Philadelphia, 1993.
8. Crookston JH, Crookston MC, Burnie KL et al. Hereditary erythroblastic multinuclearity associated with a positive acidified-serum test: a type of congenital dyserythropoietic anaemia. Br. J. Haematol. 1969; 17: 11-26.
9. Sandstrom H, Wahlin A, Eriksson M, Bergstrom I. Serum thymidine kinase in congenital dyserythropoietic anaemia type III. Br. J. Haematol. 1994; 87: 653-4.
10. Sandstrom H, Wahlin A, Eriksson M, Bergstrom I, Wickramasinghe SN. Intravascular haemolysis and increased prevalence of myeloma and monoclonal gammopathy in congenital dyserythropoietic anaemia type III. Eur. J. Haematol. 1994; 52: 42-6.
11. Miller DR. Congenital dyserythropoietic anaemia. In Miller DR, Bachm RL, McMillan CW eds. Blood Diseases of Infancy and Childhood. CV Mosby, St Louis, 1985; 200-5.
12. Halpern Z, Rahmani R, Levo Y. Severe hemochromatosis: The pre-dominant clinical manifestation of congenital dyserythropoietic anaemia type 2. Acta Hematol. 1985; 74: 178-80.