Benign familial infantile epilepsy (Q41219): Difference between revisions
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Revision as of 07:18, 13 August 2026
Epilepsy characterised by the occurrence of repeated seizures in healthy infants with no prior medical history during the first year of life. The seizures manifest with motor arrest, impairment of consciousness, staring, eye and head deviation, and mild unilateral clonic convulsions. A family history of the same epilepsy is a constant finding. The pattern of inheritance is most probably autosomal dominant.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 8A61.10 |
||
| English | Benign familial infantile epilepsy |
Epilepsy characterised by the occurrence of repeated seizures in healthy infants with no prior medical history during the first year of life. The seizures manifest with motor arrest, impairment of consciousness, staring, eye and head deviation, and mild unilateral clonic convulsions. A family history of the same epilepsy is a constant finding. The pattern of inheritance is most probably autosomal dominant. |
Statements
CID11:8A61.10
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dki-india-8A61.10
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Concluído
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13 August 2026
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