Document Detail


Progressive myoclonus epilepsies. Criteria for diagnosis on the basis of the follow-up of 37 cases.
MedLine Citation:
PMID:  1293989     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The authors report the clinical criteria for the diagnosis of progressive myoclonus epilepsies on the basis of their experience following 34 cases (2 with sialidosis, 2 with MERRF, 4 with Lafora disease, 24 with Unverricht-Lundborg type, 4 with ataxic myoclonus). 3 rare forms of PME are also reported: a case of lipoma and PME, a family with dentato-rubro-pallido-luysian atrophy and a family of myoclonus epilepsy, Hartung type. The autonomy of Ramsay Hunt syndrome is discussed on the light of recent molecular genetic data.
Authors:
G C Guazzi; A Federico
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Review    
Journal Detail:
Title:  Acta neurologica     Volume:  14     ISSN:  0001-6276     ISO Abbreviation:  Acta Neurol (Napoli)     Publication Date:    1992 Aug-Dec
Date Detail:
Created Date:  1993-04-08     Completed Date:  1993-04-08     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  0421100     Medline TA:  Acta Neurol (Napoli)     Country:  ITALY    
Other Details:
Languages:  eng     Pagination:  469-84     Citation Subset:  IM    
Affiliation:
Istituto di Scienze Neurologiche, Facoltà di Medicina e Chirurgia, Universitä degli studi di Siena.
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MeSH Terms
Descriptor/Qualifier:
Adolescent
Adult
Child
Epilepsies, Myoclonic / classification,  diagnosis*,  etiology
Female
Follow-Up Studies
Humans
Lipoma / complications
MERRF Syndrome / diagnosis,  genetics
Male
Metabolism, Inborn Errors / complications
Myoclonic Cerebellar Dyssynergia / diagnosis,  genetics
Pedigree

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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