Benign familial infantile epilepsy (Q41219): Difference between revisions
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Epilepsia caracterizada pela ocorrência de convulsões repetitivas em crianças saudáveis sem história médica prévia durante o primeiro ano de vida. As crises epilépticas se manifestam com parada motora, comprometimento da consciência, olhar fixo, desvio de olho e cabeça e convulsões clônicas unilaterais leves. História familiar da mesma epilepsia é um achado constante. O padrão de herança é mais provavelmente autossômico dominante. | |||
| description / en | description / en | ||
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. | |||
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 |
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| 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. |
