Please use this identifier to cite or link to this item: http://ahro.austin.org.au/austinjspui/handle/1/9238
Title: Epilepsy and paroxysmal movement disorders in families: evidence for shared mechanisms.
Authors: Singh, R;Macdonell, Richard A L;Scheffer, Ingrid E;Crossland, K M;Berkovic, Samuel F
Affiliation: Department of Medicine (Neurology), University of Melbourne, Austin, Australia.
Issue Date: 1-Jun-1999
Citation: Epileptic Disorders : International Epilepsy Journal With Videotape; 1(2): 93-9
Abstract: The epilepsies have been regarded as clinically distinct from the paroxysmal movement disorders. Recently, a variety of ion channel defects have been identified as the biological basis of certain familial epilepsies and paroxysmal movement disorders. We studied two families with the co-occurrence of epilepsy, movement disorders and migraine. Information was obtained on 147 individuals in the two families. In family WF, there was a co-occurrence of epilepsy (benign infantile convulsions, idiopathic generalized epilepsy), episodic ataxia (with cerebellar atrophy and without myokymia) and common migraine. In family CL, epilepsy (febrile seizures, febrile seizures plus), kinesigenic paroxysmal dyskinesia and migraine (including hemiplegic migraine) were observed in various combinations over 3 generations. The observations in these two families, together with review of the literature, suggest that the co-occurrence of epilepsy (particularly benign infantile convulsions), paroxysmal movement disorders and migraine is not due to chance. Thus, these distinct clinical phenomena could have a shared biological basis and ion channel defects are an attractive possibility.
Internal ID Number: 10937138
URI: http://ahro.austin.org.au/austinjspui/handle/1/9238
URL: http://www.ncbi.nlm.nih.gov/pubmed/10937138
Type: Journal Article
Subjects: Adolescent
Adult
Chorea.diagnosis.genetics
Diseases in Twins.genetics
Epilepsy.diagnosis.genetics
Female
Follow-Up Studies
Hemiplegia.diagnosis.genetics
Humans
Infant
Male
Middle Aged
Migraine Disorders.diagnosis.genetics
Pedigree
Phenotype
Spinocerebellar Degenerations.diagnosis.genetics
Appears in Collections:Journal articles

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