Fabry disease and sleep disorders: a systematic review

BACKGROUND: Fabry disease (FD) is an X-chromosome-linked disorder characterized by a reduced or complete absence of the enzyme α-galactosidase, resulting in the accumulation of lysosomal globotriaosylceramide. Despite the presence of these deposits in multiple organs, the problem of sleep disorders...

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Detalles Bibliográficos
Autores principales: Blaszczyk, Bartlomiej, Wieckiewicz, Mieszko, Kusztal, Mariusz, Michalek-Zrabkowska, Monika, Lachowicz, Gabriella, Mazur, Grzegorz, Martynowicz, Helena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10586315/
https://www.ncbi.nlm.nih.gov/pubmed/37869133
http://dx.doi.org/10.3389/fneur.2023.1217618

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10586315/
https://www.ncbi.nlm.nih.gov/pubmed/37869133
http://dx.doi.org/10.3389/fneur.2023.1217618

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