20p duplication (Q91022): Difference between revisions
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A trissomia 20p é um transtorno cromossômico resultante da duplicação de todo ou de parte do braço curto do cromossomo 20. É caracterizado principalmente por crescimento normal, incapacidade intelectual leve a moderada, atraso na fala, coordenação inadequada e características faciais evocativas. | |||
| description / en | description / en | ||
Trisomy 20p is a chromosomal disorder resulting from duplication of all or part of the short arm of chromosome 20. It is mostly characterised by normal growth, mild to moderate intellectual disability, speech delay, poor coordination and evocative facial features. | |||
Revision as of 18:01, 15 August 2026
Trisomy 20p is a chromosomal disorder resulting from duplication of all or part of the short arm of chromosome 20. It is mostly characterised by normal growth, mild to moderate intellectual disability, speech delay, poor coordination and evocative facial features.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1396883815 |
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| English | 20p duplication |
Trisomy 20p is a chromosomal disorder resulting from duplication of all or part of the short arm of chromosome 20. It is mostly characterised by normal growth, mild to moderate intellectual disability, speech delay, poor coordination and evocative facial features. |
