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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Bibliografiske detaljer
Udgivet i:Front Neurol
Main Authors: Barone, Rita, Fiumara, Agata, Gulisano, Mariangela, Cirnigliaro, Lara, Cocuzza, Maria Donatella, Guida, Claudia, Pettinato, Fabio, Greco, Filippo, Elia, Maurizio, Rizzo, Renata
Format: Artigo
Sprog:Inglês
Udgivet: Frontiers Media S.A. 2021
Fag:
Neurology
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC8326392/
https://ncbi.nlm.nih.gov/pubmed/34349725
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2021.705423
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