| Literature DB >> 17994571 |
Cécile Alanio-Bréchot1, Pierre-Olivier Schischmanoff, Madeleine Fénéant-Thibault, Thérèse Cynober, Gil Tchernia, Jean Delaunay, Loïc Garçon.
Abstract
Constitutional deficit in the erythroid protein 4.1 (4.1R), a structural component of the erythrocyte membrane, is implicated in hereditary elliptocytosis. Acquired deficit in protein 4.1R have been rarely described in myelodysplastic syndromes. Here, we report a series of six patients presenting a myelodysplastic or a myeloproliferative disease in association with an elliptocytosis curve on osmotic gradient ektacytometry and a significant decrease in protein 4.1R level. We confirm that deficit in protein 4.1R is recurrent in myeloid malignancies and should be particularly investigated when deletion del (20 q) is present, since we found this chromosomal abnormality in four out of six patients. (c) 2007 Wiley-Liss, Inc.Entities:
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Year: 2008 PMID: 17994571 DOI: 10.1002/ajh.21088
Source DB: PubMed Journal: Am J Hematol ISSN: 0361-8609 Impact factor: 10.047