10p duplication (Q85271): Difference between revisions

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A duplicação 10p (trissomia 10p) é uma síndrome de incapcidade intelectual/malformações congênitas múltiplas (MR-MCA) que é causada pela duplicação total ou parcial do braço curto do cromossomo 10 e que resulta em um dismorfismo facial distinto, deficiências intelectual e motora graves, hipotonia muscular e hipotrofia e anomalias variáveis incluindo anomalias osteoarticulares, cardíacas, renais e oculares.
description / endescription / en
 
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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Property / Canonical URI: https://id.who.int/icd/entity/442413368 / rank
 
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CID11:ID_442413368
Property / CURIE: CID11:ID_442413368 / rank
 
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dki-india-ID_442413368
Property / Canary Token: dki-india-ID_442413368 / rank
 
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Concluído
Property / Verification Status: Concluído / rank
 
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Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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13 August 2026
Timestamp+2026-08-13T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
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Property / Collection date: 13 August 2026 / rank
 
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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.
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ID_442413368
    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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