Mucopolysaccharidoses I and II: Brief Review of Therapeutic Options and Supportive/Palliative Therapies

Purpose. Mucopolysaccharidoses (MPS) are group of inherited lysosomal storage diseases caused by mutations of enzymes involved in catalyzing different glycosaminoglycans (GAGs). MPS I and MPS II exhibit both somatic and neurological symptoms with a relatively high disease incidence. Hematopoietic st...

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Detalles Bibliográficos
Autores principales: Nan, Haiyan, Park, Chanbum, Maeng, Sungho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7732385/
https://www.ncbi.nlm.nih.gov/pubmed/33344633
http://dx.doi.org/10.1155/2020/2408402

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7732385/
https://www.ncbi.nlm.nih.gov/pubmed/33344633
http://dx.doi.org/10.1155/2020/2408402

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