Hereditary elliptocytosis (Q39534): Difference between revisions
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A eliptocitose hereditária é um grupo de doenças raras causada por anormalidades no citoesqueleto do glóbulo vermelho e evidenciao pela presença no esfregaço sanguíneo de numerosos glóbulos vermelhos elípticos, denominados eliptócitos. As apresentações clínicas são altamente heterogeneas variando de formas assintomáticas a formas mais graves associadas com anemia variável, de moderada a grave e com piropoiquilocitose incluindo eritrócitos fragmentados, microeliptócitos e microesferócitos | |||||||||||||||
| description / en | description / en | ||||||||||||||
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. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/679955609 / rank | |||||||||||||||
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CID11:3A10.2 | |||||||||||||||
| Property / CURIE: CID11:3A10.2 / rank | |||||||||||||||
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dki-india-3A10.2 | |||||||||||||||
| Property / Canary Token: dki-india-3A10.2 / rank | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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13 August 2026
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| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
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| Property / Linked ICD 10: D58.1 / rank | |||||||||||||||
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Latest 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 |
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| 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. |
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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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