10p duplication (Q85271): Difference between revisions
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13 August 2026
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Latest revision as of 10:38, 15 August 2026
10p duplication (Trisomy 10p) is a syndrome of mental retardation/multiple congenital malformations (MR-MCA) that is caused by the total or partial duplication of the short arm of chromosome 10 and that results in a distinctive facial dysmorphism, severe intellectual and motor deficiency, muscular hypotonia and hypotrophy and variable anomalies including osteoarticular, cardiac, renal and ocular anomalies.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_442413368 |
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| English | 10p duplication |
10p duplication (Trisomy 10p) is a syndrome of mental retardation/multiple congenital malformations (MR-MCA) that is caused by the total or partial duplication of the short arm of chromosome 10 and that results in a distinctive facial dysmorphism, severe intellectual and motor deficiency, muscular hypotonia and hypotrophy and variable anomalies including osteoarticular, cardiac, renal and ocular anomalies. |
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CID11:ID_442413368
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dki-india-ID_442413368
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Concluído
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13 August 2026
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