Lafora body disease: clinical features
Evidence-based neurology checklist on lafora body disease: clinical features: Onset The onset age is usually 12-17 years: the range is 6-22 years Onset after the age of 50 years has been reported Seizure types Psychiatric features Cognitive features Other features Clinical course Differential…
Onset
- The onset age is usually 12-17 years: the range is 6-22 years
- Onset after the age of 50 years has been reported
Seizure types
Psychiatric features
Cognitive features
Other features
Clinical course
Differential diagnosis (of progressive myoclonus epilepsy)
References
- Chan EM, Omer S, Ahmed M, et al. Progressive myoclonus epilepsy with polyglucosans (Lafora disease): evidence for a third locus. Neurology 2004; 63:565-567.
- Lohi H, Turnbull J, Zhao XC, et al. Genetic diagnosis in Lafora disease: genotype-phenotype correlations and diagnostic pitfalls. Neurology 2007; 68:996-1001.
- Franceschetti S, Michelucci R, Canafoglia L, et al. Progressive myoclonic epilepsies: definitive and still undetermined causes. Neurology 2014; 82:405-411.
- Andrade DM, Turnbull J, Minassian BA. Lafora disease, seizures and sugars. Acta Myol 2007; 26:83-86.
- Turnbull J, Girard JM, Lohi H, et al. Early-onset Lafora body disease. Brain 2012; 135:2684-2698.
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