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Congenital dyserythropoietic anemias.

作者信息

Wickramasinghe S N

机构信息

Department of Hematology, Imperial College School of Medicine, London, UK.

出版信息

Curr Opin Hematol. 2000 Mar;7(2):71-8. doi: 10.1097/00062752-200003000-00001.

DOI:10.1097/00062752-200003000-00001
PMID:10698292
Abstract

The congenital dyserythropoietic anemias (CDAs) are an uncommon and heterogeneous group of disorders characterized by markedly ineffective erythropoiesis and, usually, striking dysplastic changes in erythroblasts. Each of the three originally described forms, designated CDA types I to III, is defined by the presence of distinctive morphologic (including ultrastructural) abnormalities in erythroblasts. CDA type II is also characterized by a marked reduction in polylactosamine structures associated with the erythrocyte membrane glycoprotein, band 3 (detected by sodium dodecyl sulfate polyacrylamide gel electrophoresis), and, usually, a positive result on the acidified serum lysis test. The course of CDA is often complicated by cholelithiasis. Even patients who have not had transfusions sometimes develop substantial iron overload. Recent studies have extended our knowledge on the clinical manifestations of CDA types I and III and have revealed the existence of forms of CDA distinct from types I to III. Information is now available on the chromosomal localization of the genes involved in CDA types I and II and in the Swedish cases of CDA type III. A few patients with CDA type I have been treated with interferon-alpha2, with a good response.

摘要

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引用本文的文献

1
Congenital dyserythropoietic anaemia type II: a rare entity.II型先天性红细胞生成异常性贫血:一种罕见病症。
BMJ Case Rep. 2011 Apr 19;2011:bcr0120113684. doi: 10.1136/bcr.01.2011.3684.
2
Molecular analysis of 42 patients with congenital dyserythropoietic anemia type II: new mutations in the SEC23B gene and a search for a genotype-phenotype relationship.对 42 例先天性红细胞生成性贫血Ⅱ型患者的分子分析:SEC23B 基因突变及基因型-表型关系的研究。
Haematologica. 2010 May;95(5):708-15. doi: 10.3324/haematol.2009.014985. Epub 2009 Dec 16.
3
Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II.
影响分泌性COPII包被组分SEC23B的突变会导致II型先天性红细胞生成异常性贫血。
Nat Genet. 2009 Aug;41(8):936-40. doi: 10.1038/ng.405. Epub 2009 Jun 28.