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- Gahrton, G, et al.
(författare)
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Stamcellstransplantation
- 2012
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Ingår i: Westin J. (ed) Femtio år med svensk hematologi, en krönika om människor och miljöer, sjukvård och forskning. - 9789163714252 ; , s. 46-60
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Bokkapitel (övrigt vetenskapligt/konstnärligt)
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- Sandström, Herbert, et al.
(författare)
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[Localized gene of the rare "Norrland disease". CDA-III blood disease with dominant heredity].
- 1999
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Ingår i: Läkartidningen. - 0023-7205 .- 1652-7518. ; 96:4, s. 343-7
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Tidskriftsartikel (refereegranskat)abstract
- 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.
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