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Lafora disease: A progressive myoclonus epilepsy

✍ Scribed by E. J. ELLIOTT; I. C. TALBOT; I. F. PYE; S. HODGES; P. G. F. SWIFT; M. S. TANNER

Book ID
118706620
Publisher
John Wiley and Sons
Year
1992
Tongue
English
Weight
804 KB
Volume
28
Category
Article
ISSN
1034-4810

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πŸ“œ SIMILAR VOLUMES

Lafora progressive myoclonus epilepsy:NH
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Lafora disease 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 ar

Lafora progressive myoclonus epilepsy mu
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Communicated by Alastair F. Brown Progressive Myoclonus Epilepsy (PME) of the Lafora type is an autosomal recessive disease, which presents in teenage years with myoclonia and generalized seizures leading to death within a decade of onset. It is characterized by pathognomonic inclusions, Lafora bodi