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31 de jul. de 2023 · Lennox-Gastaut syndrome (LGS) is a rare but severe form of childhood epilepsy characterized by a triad of multiple seizure types, characteristic EEG findings, and intellectual impairment. It is one of the epileptic encephalopathies.
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The Curious Case of Lennox-Gastaut Syndrome:...
- Lennox-Gastaut Syndrome: In a Nutshell
Lennox-Gastaut syndrome is one of the rare childhood-onset...
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5 de jun. de 2023 · CLASSIFICATION. LGS is considered a severe developmental epileptic encephalopathy, in which seizure activity and epileptic discharges cause or contribute to severe cognitive impairment and behavioral disorders beyond what would be expected from the underlying etiology [ 3 ]. ETIOLOGY.
Definición de la enfermedad. Es una encefalopatía epiléptica del desarrollo poco frecuente, grave y de inicio temprano, caracterizada por la tríada de deficiencia intelectual, múltiples tipos de crisis epilépticas y anomalías características en el electroencefalograma (EEG). ORPHA:2382. Nivel de clasificación: Trastorno. Prevalencia: 1-5 / 10 000.
28 de nov. de 2023 · What is Lennox-Gastaut syndrome? Lennox-Gastaut syndrome is a severe form of epilepsy. Seizures begin in early childhood, usually before the age of 4 years. Children, adolescents, and adults with Lennox-Gastaut syndrome have multiple types of seizures that vary among individuals. Common seizure types include:
Abstract. Lennox-Gastaut syndrome (LGS) is considered an epileptic encephalopathy and is defined by a triad of multiple drug-resistant seizure types, a specific EEG pattern showing bursts of slow spike-wave complexes or generalized paroxysmal fast activity, and intellectual disability.
Lennox-Gastaut syndrome (LGS) is a severe form of epilepsy with childhood onset. LGS can occur as a secondary result of an insult to the brain either during the prenatal, perinatal, or neonatal periods, or can occur in an otherwise previously healthy child.
