Complete trisomy 21 (Q46751): Difference between revisions
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Latest revision as of 15:33, 13 August 2026
Trisomy 21 is a chromosomal abnormality, characterised by the presence of a third (partial or total) copy of chromosome 21, which clinical manifestations include variable intellectual deficiency, muscular hypotonia and joint laxity, often associated with facial dysmorphism and variable malformations (essentially heart and digestive) and a risk of complications (epilepsy, leukemia, auto-immune and endocrine pathologies, earlier aging and Alzheimer disease.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LD40.0 |
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| English | Complete trisomy 21 |
Trisomy 21 is a chromosomal abnormality, characterised by the presence of a third (partial or total) copy of chromosome 21, which clinical manifestations include variable intellectual deficiency, muscular hypotonia and joint laxity, often associated with facial dysmorphism and variable malformations (essentially heart and digestive) and a risk of complications (epilepsy, leukemia, auto-immune and endocrine pathologies, earlier aging and Alzheimer disease. |
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CID11:LD40.0
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dki-india-LD40.0
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Concluído
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13 August 2026
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