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Juvenile myoclonic epilepsy starting in the eighth decade

Tóth, Vanda and Rasonyi, György and Fogarasi, András and Kovács, Norbert and Auer, Tibor and Janszky, József Vladimír (2007) Juvenile myoclonic epilepsy starting in the eighth decade. EPILEPTIC DISORDERS, 9 (3). pp. 341-345. ISSN 1294-9361

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Abstract

Juvenile myoclonic epilepsy (JME) typically begins at age 10-17 years. We present two patients, with no previous history of epileptic seizures, in whom JME began after the age of 70. The clinical picture of these patients did not differ from "typical" JME except for the patient's age and age at epilepsy-onset. We suggest that not only symptomatic epilepsy, but also some idiopathic epilepsies, can begin or can be reactivated in elderly people. This may be more evidence that susceptibility to epileptic seizures is increased after 60 years of age.

Item Type: Article
Uncontrolled Keywords: Valproic Acid/therapeutic use; Myoclonic Epilepsy, Juvenile/*physiopathology; Male; Magnetic Resonance Imaging; Humans; Female; Epilepsy, Tonic-Clonic/physiopathology; Electroencephalography; Anticonvulsants/therapeutic use; Aged
Subjects: R Medicine / orvostudomány > RC Internal medicine / belgyógyászat > RC0321 Neuroscience. Biological psychiatry. Neuropsychiatry / idegkórtan, neurológia, pszichiátria
SWORD Depositor: MTMT SWORD
Depositing User: MTMT SWORD
Date Deposited: 20 May 2015 08:01
Last Modified: 20 May 2015 08:01
URI: http://real.mtak.hu/id/eprint/24135

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