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Erschienen in: CNS Drugs 7/2010

01.07.2010 | Therapy in Practice

Lafora disease

Epidemiology, pathophysiology and management

verfasst von: Thomas S. Monaghan, Dr Norman Delanty

Erschienen in: CNS Drugs | Ausgabe 7/2010

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Abstract

Lafora disease is a rare, fatal, autosomal recessive, progressive myoclonic epilepsy. It may also be considered as a disorder of carbohydrate metabolism because of the formation of polyglucosan inclusion bodies in neural and other tissues due to abnormalities of the proteins laforin or malin. The condition is characterized by epilepsy, myoclonus and dementia. Diagnostic findings on MRI and neurophysiological testing are not definitive and biopsy or genetic studies may be required. Therapy in Lafora disease is currently limited to symptomatic management of the epilepsy, myoclonus and intercurrent complications. With a greater understanding of the pathophysiological processes involved, there is justified hope for future therapies.
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Metadaten
Titel
Lafora disease
Epidemiology, pathophysiology and management
verfasst von
Thomas S. Monaghan
Dr Norman Delanty
Publikationsdatum
01.07.2010
Verlag
Springer International Publishing
Erschienen in
CNS Drugs / Ausgabe 7/2010
Print ISSN: 1172-7047
Elektronische ISSN: 1179-1934
DOI
https://doi.org/10.2165/11319250-000000000-00000

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