Epilepsy with myoclonic-astatic seizures (Q41211): Difference between revisions

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Epilepsia iniciando entre o segundo e quinto ano de vida em uma criança previamente normal com história familiar de convulsões, que inicialmente se manifesta com convulsões tônico-clônicas e com crises mioclônicas-astáticas começando várias semanas depois. Estas convulsões são caracterizadas por súbita perda do tônus mucular associada a propulsão para frente ou para trás que podem resultar em lesão de face e cabeça se o paciente cair.
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Epilepsy beginning between the second and fifth year of life in a previously normal child with family history of seizures, that initially manifests as tonic-clonic seizures with myoclonic-astatic seizures beginning several weeks later. These seizures are characterised by a sudden loss of muscular tonus associated with forward or backward propulsion that may result in injury to the face and head if the patient falls.

Revision as of 07:17, 13 August 2026

Epilepsy beginning between the second and fifth year of life in a previously normal child with family history of seizures, that initially manifests as tonic-clonic seizures with myoclonic-astatic seizures beginning several weeks later. These seizures are characterised by a sudden loss of muscular tonus associated with forward or backward propulsion that may result in injury to the face and head if the patient falls.
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8A61.22
    English
    Epilepsy with myoclonic-astatic seizures
    Epilepsy beginning between the second and fifth year of life in a previously normal child with family history of seizures, that initially manifests as tonic-clonic seizures with myoclonic-astatic seizures beginning several weeks later. These seizures are characterised by a sudden loss of muscular tonus associated with forward or backward propulsion that may result in injury to the face and head if the patient falls.

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