| Literature DB >> 10971401 |
N Parez1, M Dommergues, V Zupan, H Chambost, J B Fieschi, J Delaunay, F Miélot, E M Cramer, J P Dommergues, S N Wickramasinghe, G Tchernia.
Abstract
We report a case of congenital dyserythropoietic anaemia, type I, with severe pre- and postnatal manifestations. Exchange transfusions were required for fetal anaemia (3.5 g/dl) at 28 and 30 weeks of gestation. Transfusions were administered at birth (Caesarean section at week 35) and at regular intervals thereafter. At 14 months, alpha-interferon therapy was initiated (106 units three times a week). This resulted in stabilization of the haemoglobin at or above 11 g/dl and a reduction in the percentage of erythroblasts with ultrastructurally abnormal heterochromatin. After 9 months, the dose of alpha-interferon was decreased to 106 units twice a week. No relapse of anaemia was noted during an additional 4 months of follow-up.Entities:
Mesh:
Substances:
Year: 2000 PMID: 10971401 DOI: 10.1046/j.1365-2141.2000.02168.x
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998