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[Localized gene of the rare "Norrland disease". CDA-III blood disease with dominant heredity].
Umeå University, Faculty of Medicine, Department of Public Health and Clinical Medicine, Family Medicine.
1999 (Swedish)In: Läkartidningen, ISSN 0023-7205, E-ISSN 1652-7518, Vol. 96, no 4, 343-7 p.Article in journal (Refereed) Published
Abstract [sv]

The article consists in a review of available knowledge of the rare blood disorder, congenital dyserythropoietic anaemia, type III (CDA-III), a disease characterised by autosomal dominant heredity, and mild to moderate haemolytic anaemia. The gene causing CDA-III has been localised on chromosome 15q22. Most patients are adapted to their disease, and have few or no overt manifestations. Bone marrow examination yields a characteristic picture of erythroid hyperplasia and multinucleate erythroblasts. A Swedish family affected with CDA-III has been reported to be characterised by a high prevalence of monoclonal gammopathy and angioid streaks, a triad suggested by the authors to represent a hitherto unreported syndrome.

Place, publisher, year, edition, pages
1999. Vol. 96, no 4, 343-7 p.
National Category
Medical and Health Sciences
Identifiers
URN: urn:nbn:se:umu:diva-66831PubMedID: 10024825OAI: oai:DiVA.org:umu-66831DiVA: diva2:609417
Available from: 2013-03-05 Created: 2013-03-05 Last updated: 2017-12-06

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