Natural history of Lafora disease: a prognostic systematic review and individual participant data meta-analysis

BACKGROUND: Lafora disease (LD) is a rare fatal autosomal recessive form of progressive myoclonus epilepsy. It affects previously healthy children or adolescents, causing pharmacoresistant epilepsy, myoclonus and severe psychomotor deterioration. This work aims to describe the clinical course of LD...

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Detalles Bibliográficos
Autores principales: Pondrelli, Federica, Muccioli, Lorenzo, Licchetta, Laura, Mostacci, Barbara, Zenesini, Corrado, Tinuper, Paolo, Vignatelli, Luca, Bisulli, Francesca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8365996/
https://www.ncbi.nlm.nih.gov/pubmed/34399803
http://dx.doi.org/10.1186/s13023-021-01989-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8365996/
https://www.ncbi.nlm.nih.gov/pubmed/34399803
http://dx.doi.org/10.1186/s13023-021-01989-w

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