Congenital dyserythropoietic anaemia (Q39569): Difference between revisions
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13 August 2026
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Latest revision as of 05:02, 13 August 2026
Congenital dyserythropoietic anaemias (CDA) result from diverse erythropoietic disorders; they lead to the defective production of red blood cells (RBC) and often mild haemolysis that attests to a qualitative defect of these RBC released into the circulation. Three forms of CDA have been characterised: types I, II and III. The shared symptoms include anaemia of variable severity, intermittent jaundice, splenomegaly and hepatomegaly.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 3A73 |
||
| English | Congenital dyserythropoietic anaemia |
Congenital dyserythropoietic anaemias (CDA) result from diverse erythropoietic disorders; they lead to the defective production of red blood cells (RBC) and often mild haemolysis that attests to a qualitative defect of these RBC released into the circulation. Three forms of CDA have been characterised: types I, II and III. The shared symptoms include anaemia of variable severity, intermittent jaundice, splenomegaly and hepatomegaly. |
Statements
CID11:3A73
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dki-india-3A73
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Concluído
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13 August 2026
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