Hereditary elliptocytosis (Q39534): Difference between revisions
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Revision as of 04:59, 13 August 2026
Hereditary elliptocytosis is a group of rare conditions caused by abnormalities in the red cell cytoskeleton and marked by the presence on blood smears of numerous elliptical red blood cells, called elliptocytes. Clinical presentations are highly heterogeneous ranging from asymptomatic forms to more severe forms associated with variable anaemia, from moderate to severe and with pyropoikilocytosis including fragmented red cells, microelliptocytes and microspherocytes.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 3A10.2 |
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| English | Hereditary elliptocytosis |
Hereditary elliptocytosis is a group of rare conditions caused by abnormalities in the red cell cytoskeleton and marked by the presence on blood smears of numerous elliptical red blood cells, called elliptocytes. Clinical presentations are highly heterogeneous ranging from asymptomatic forms to more severe forms associated with variable anaemia, from moderate to severe and with pyropoikilocytosis including fragmented red cells, microelliptocytes and microspherocytes. |
Statements
CID11:3A10.2
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dki-india-3A10.2
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Concluído
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13 August 2026
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