15q11 duplication or inversion (Q85727): Difference between revisions
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Síndrome de duplicação/inversão 15q11 ou cromossomo 15 isodicêntrico (inv dup(15) ou idic(15)) é um transtorno cromossômico com achados clínicos distintos, caracterizado por hipotonia central precoce, atraso no desenvolvimento e déficit intelectual, epilepsia e comportamento autista. | |||
| description / en | description / en | ||
The duplication/inversion 15q11 or isodicentric 15 chromosome (inv dup(15) or idic(15)) syndrome is a chromosomal disorder with distinctive clinical findings characterised by early central hypotonia, developmental delay and intellectual deficit, epilepsy, and autistic behaviour. | |||
Revision as of 11:05, 15 August 2026
The duplication/inversion 15q11 or isodicentric 15 chromosome (inv dup(15) or idic(15)) syndrome is a chromosomal disorder with distinctive clinical findings characterised by early central hypotonia, developmental delay and intellectual deficit, epilepsy, and autistic behaviour.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1920979014 |
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| English | 15q11 duplication or inversion |
The duplication/inversion 15q11 or isodicentric 15 chromosome (inv dup(15) or idic(15)) syndrome is a chromosomal disorder with distinctive clinical findings characterised by early central hypotonia, developmental delay and intellectual deficit, epilepsy, and autistic behaviour. |
