Epilepsy due to autosomal dominant genetic syndromes with widespread or progressive effects (Q86434)
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Epilepsy due to a wide variety of clinical conditions having in common an autosomal dominant genetic defect. Phenotype varies with the age of the patient. Seizure semiology and electroencephalographic features are indistinguishable. Excludes genetic syndromes primarily expressed as epilepsy.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1970837340 |
||
| English | Epilepsy due to autosomal dominant genetic syndromes with widespread or progressive effects |
Epilepsy due to a wide variety of clinical conditions having in common an autosomal dominant genetic defect. Phenotype varies with the age of the patient. Seizure semiology and electroencephalographic features are indistinguishable. Excludes genetic syndromes primarily expressed as epilepsy. |
Statements
CID11:ID_1970837340
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dki-india-ID_1970837340
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Concluído
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13 August 2026
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