Epilepsy due to X-linked recessive progressive myoclonic epilepsy with ataxia (Q86435)
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Epilepsy due to a wide variety of clinical conditions having in common an X-linked 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_1252358703 |
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| English | Epilepsy due to X-linked recessive progressive myoclonic epilepsy with ataxia |
Epilepsy due to a wide variety of clinical conditions having in common an X-linked 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_1252358703
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dki-india-ID_1252358703
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Concluído
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13 August 2026
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