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Lennox s. an atypical form of absence epilepsy characterized by diffuse slow spike waves, often with atonic, tonic, or clonic seizures and mental retardation; there may also be other neurological abnormalities or multiple seizure types. Unlike typical absence epilepsy, it may persist into adulthood. Called also petit mal variant.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
Lennox-Gastaut syndrome A difficult-to-treat disorder beginning in childhood, characterized by multiple seizure types, including drop attacks, absence and tonic-clonic seizures. Mental retardation is common and often progressive.
Ãâó: www.epilepsysandiego.org/common_terms.htm
Lennox-Gastaut syndrome epilepsy Epilepsy with onset in early childhood. This type of epilepsy is characterized by a variety of seizure patterns and an abnormal electroencephalogram, and is frequently associated with developmental and mental ret
Ãâó:
Lennox-Gastaut syndrome a severe, common form of epilepsy which usually consists of multiple, difficult to control seizure types, slow generalized spike and wave on EEG (2 cycles per second), usually developmental delay. Of note is that 10% of patients do not have developmental delay.
Ãâó: www.epipro.com/defin.html
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