Single seizure due to genetic syndromes with widespread or progressive effects (Q83756): Difference between revisions
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Convulsão não provocada ocorrendo em paciente com uma condição geneticamente determinada em que a epilepsia coexiste com incapacidade intelectual e/ou características dismórficas. Inclui crises epilépticas devidas a anormalidades autossômicas, ligadas ao X, mitocondriais ou cromossômicas. | |||
| description / en | description / en | ||
An unprovoked seizure occurring in a patient with a genetically determined condition in which epilepsy coexists with mental retardation and/or dysmorphic features. Includes seizures due to autosomal, X-linked, mitochondrial or chromosomal abnormalities. | |||
Revision as of 09:07, 15 August 2026
An unprovoked seizure occurring in a patient with a genetically determined condition in which epilepsy coexists with mental retardation and/or dysmorphic features. Includes seizures due to autosomal, X-linked, mitochondrial or chromosomal abnormalities.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_734748791 |
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| English | Single seizure due to genetic syndromes with widespread or progressive effects |
An unprovoked seizure occurring in a patient with a genetically determined condition in which epilepsy coexists with mental retardation and/or dysmorphic features. Includes seizures due to autosomal, X-linked, mitochondrial or chromosomal abnormalities. |
