Epilepsy due to genetic syndromes with widespread or progressive effects (Q41194): Difference between revisions
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Revision as of 07:15, 13 August 2026
Epilepsy due to genetically determined conditions in which, as we currently understand it, there is a separate disorder interposed between the genetic defect and the epilepsy, for example, as in tuberous sclerosis. Includes epilepsy due to documented autosomal, X-linked, mitochondrial or chromosomal abnormalities.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 8A60.A |
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| English | Epilepsy due to genetic syndromes with widespread or progressive effects |
Epilepsy due to genetically determined conditions in which, as we currently understand it, there is a separate disorder interposed between the genetic defect and the epilepsy, for example, as in tuberous sclerosis. Includes epilepsy due to documented autosomal, X-linked, mitochondrial or chromosomal abnormalities. |
