Electroclinical Features of Epilepsy in Mucopolysaccharidosis III: Outcome Description in a Cohort of 15 Italian Patients

Mucopolysaccharidosis III (Sanfilippo syndromes) types A–D are rare lysosomal storage disorders characterized by heparan sulfate accumulation and neurodegeneration. Patients with MPS III present with developmental stagnation and/or regression, sleep disturbance, and behavioral abnormalities usually...

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Detalles Bibliográficos
Autores principales: Barone, Rita, Fiumara, Agata, Gulisano, Mariangela, Cirnigliaro, Lara, Cocuzza, Maria Donatella, Guida, Claudia, Pettinato, Fabio, Greco, Filippo, Elia, Maurizio, Rizzo, Renata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8326392/
https://www.ncbi.nlm.nih.gov/pubmed/34349725
http://dx.doi.org/10.3389/fneur.2021.705423

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8326392/
https://www.ncbi.nlm.nih.gov/pubmed/34349725
http://dx.doi.org/10.3389/fneur.2021.705423

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