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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Bibliographic Details
Main Authors: Rita Barone, Agata Fiumara, Mariangela Gulisano, Lara Cirnigliaro, Maria Donatella Cocuzza, Claudia Guida, Fabio Pettinato, Filippo Greco, Maurizio Elia, Renata Rizzo
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-07-01
Series:Frontiers in Neurology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fneur.2021.705423/full