An unusual variant of congenital dyserythropoietic anaemia with mild maternal and lethal fetal disease
- 1 July 1993
- journal article
- Published by Wiley in British Journal of Haematology
- Vol. 84 (3) , 549-551
- https://doi.org/10.1111/j.1365-2141.1993.tb03119.x
Abstract
Summary. An unusual variant of congenital dyserythropoietic anaemia is described presenting as mild haemolytic anaemia with multinucleated erythroblasts in the marrow of the proband. The outcome of her non-consanguineous pregnancy was a third trimester, in utero, fetal demise. The hydropic fetus had dyserythropoiesis with circulating multi-nucleated erythroblasts, and haemosiderosis. Re-evaluation of the proband revealed a variant of congenital dyserythropoietic anaemia with an inheritance pattern, and with morphological, serological and biochemical features which are not consistent with any of the three described variants of congenital dyserythropoietic anaemias.Keywords
This publication has 7 references indexed in Scilit:
- A VAKIANT CONGENITAL DYSERYTHROPOIETIC ANAEMIA PRESENTING AS A FATAL HYDROPS FOETALISBritish Journal of Haematology, 1990
- A CONGENITAL DYSERYTHROPOIETIC ANAEMIA VARIANT PRESENTING AS HYDROPS FOETALISBritish Journal of Haematology, 1989
- Defective glycosylation of erythrocyte membrane glycoconjugates in a variant of congenital dyserythropoietic anemia type II: association of low level of membrane-bound form of galactosyltransferaseBlood, 1989
- Primary defect of congenital dyserythropoietic anemia type II. Failure in glycosylation of erythrocyte lactosaminoglycan proteins caused by lowered N-acetylglucosaminyltransferase II.Journal of Biological Chemistry, 1987
- Mechanisms of Immune Lysis of the Red Cells in Hereditary Erythroblastic Multinuclearity with a Positive Acidified Serum Test and Paroxysmal Nocturnal HemoglobinuriaJournal of Clinical Investigation, 1974
- Congenital Dyserythropoietic Anemia Type II: Ultrastructural and Radioautographic Studies of Blood and Bone MarrowBlood, 1972