Kleefstra syndrome (Q94178): Difference between revisions
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Síndrome de Kleefstra é um transtorno genético caracterizado por incapacidade intelectual, hipotonia infantil, grave atraso expressivo na fala e uma aparência facial distinta com um espectro de características clínicas adicionais. | |||
| description / en | description / en | ||
Kleefstra syndrome is a genetic disorder characterised by intellectual disability, childhood hypotonia, severe expressive speech delay and a distinctive facial appearance with a spectrum of additional clinical features. | |||
Revision as of 09:18, 16 August 2026
Kleefstra syndrome is a genetic disorder characterised by intellectual disability, childhood hypotonia, severe expressive speech delay and a distinctive facial appearance with a spectrum of additional clinical features.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1997337437 |
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| English | Kleefstra syndrome |
Kleefstra syndrome is a genetic disorder characterised by intellectual disability, childhood hypotonia, severe expressive speech delay and a distinctive facial appearance with a spectrum of additional clinical features. |
