Peripheral neuropathy in metachromatic leukodystrophy: current status and future perspective

Metachromatic leukodystrophy (MLD) is an autosomal recessively inherited metabolic disease characterized by deficient activity of the lysosomal enzyme arylsulfatase A. Its deficiency results in accumulation of sulfatides in neural and visceral tissues, and causes demyelination of the central and per...

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Detalles Bibliográficos
Autores principales: Beerepoot, Shanice, Nierkens, Stefan, Boelens, Jaap Jan, Lindemans, Caroline, Bugiani, Marianna, Wolf, Nicole I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829806/
https://www.ncbi.nlm.nih.gov/pubmed/31684987
http://dx.doi.org/10.1186/s13023-019-1220-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829806/
https://www.ncbi.nlm.nih.gov/pubmed/31684987
http://dx.doi.org/10.1186/s13023-019-1220-4

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