Congenital dyserythropoietic anaemia (Q39569): Difference between revisions
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Anemias diseritropoiéticas congênitas (ADC) resultam de diversos transtornos eritropoiéticos; eles levam a uma produção defeituosa de glóbulos vermelhos (GV) e, frequentemente, a hemólise leve, o que confirma um defeito qualitativo desses GV liberados na circulação. Foram caracterizadas três formas de ADC: tipos I, II e III. Os sintomas compartilhados incluem anemia de gravidade variável, icterícia intermitente, esplenomegalia e hepatomegalia. | |||
| description / en | description / en | ||
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. | |||
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 |
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| 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. |
