Lafora Progressive Myoclonus Epilepsy: Recent Insights into Cell Degeneration

Author(s): Carlos Spuch, Saida Ortolano, Carmen Navarro

Journal Name: Recent Patents on Endocrine, Metabolic & Immune Drug Discovery
Continued as New Advances on Endocrine Metabolic and Immune Diseases

Volume 6 , Issue 2 , 2012


Lafora disease (LD) is a fatal autosomal recessive form of progressive myoclonus epilepsy. Patients manifest myoclonus and tonic-clonic seizures, visual hallucinations, intellectual, and progressive neurologic deterioration beginning in adolescence. The two genes known to be involved in Lafora disease are EPM2A and NHLRC1 (EPM2B). The EPM2A gene encodes laforin, a dual-specificity protein phosphatase, and the NHLRC1 gene encodes malin, an E3- ubiquitin ligase. The two proteins interact with each other and, as a complex, are thought to regulate glycogen synthesis. 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 review also outlines important patents related to Lafora disease.

Keywords: Brain, brain diseases, central nervous system, lafora disease, laforin, malin, neurodegenerative diseases, autosomal recessive, Lafora disease, glycogen synthase activity

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Article Details

Year: 2012
Published on: 09 May, 2012
Page: [99 - 107]
Pages: 9
DOI: 10.2174/187221412800604617
Price: $65

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