Progressive myoclonus epilepsy with polyglucosan bodies: Lafora disease

Adv Neurol. 2002:89:199-210.

Author

Berge A Minassian¹

Affiliation

¹ Department of Pediatrics (Neurology), Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.

PMID: 11968446

No abstract available

Publication types

Review

MeSH terms

Brain / pathology
Brain / physiopathology
Diagnosis, Differential
Disease Progression
Glucans / metabolism
Humans
Lafora Disease / diagnosis
Lafora Disease / genetics
Lafora Disease / pathology
Lafora Disease / physiopathology*
Mutation
Protein Tyrosine Phosphatases / genetics
Protein Tyrosine Phosphatases / metabolism
Protein Tyrosine Phosphatases, Non-Receptor
Spinal Cord / pathology

Substances

Glucans
polyglucosan
Protein Tyrosine Phosphatases
Protein Tyrosine Phosphatases, Non-Receptor
EPM2A protein, human