Juvenile myoclonic epilepsy: under-appreciated and under-diagnosed.

Abstract:

:Juvenile myoclonic epilepsy (JME) is a hereditary, idiopathic, generalised epilepsy and is found in 5%-11% of patients with epilepsy. It is characterised by myoclonic jerks, occasional generalised tonic-clonic seizures, and sometimes absence seizures. JME continues to be under-appreciated and under-diagnosed. Accurate diagnosis is important as it usually responds well to treatment with appropriate anticonvulsants and misdiagnosis often results in unnecessary morbidity. In addition lifelong therapy is usually indicated as the natural history is one of relapse off treatment, even after a prolonged seizure-free period.

journal_name

Postgrad Med J

authors

Renganathan R,Delanty N

doi

10.1136/pmj.79.928.78

subject

Has Abstract

pub_date

2003-02-01 00:00:00

pages

78-80

issue

928

eissn

0032-5473

issn

1469-0756

journal_volume

79

pub_type

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