Gastrointestinal Manifestations in Mucopolysaccharidosis Type III: Review of Death Certificates and the Literature

Background: Mucopolysaccharidosis type III (MPS III, Sanfilippo disease) is a life-limiting recessive lysosomal storage disorder caused by a deficiency in the enzymes involved in degrading glycosaminoglycan heparan sulfate. MPS III is characterized by progressive deterioration of the central nervous...

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Detalles Bibliográficos
Autores principales: Thomas, Sophie, Ramaswami, Uma, Cleary, Maureen, Yaqub, Medeah, Raebel, Eva M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8509825/
https://www.ncbi.nlm.nih.gov/pubmed/34640463
http://dx.doi.org/10.3390/jcm10194445

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8509825/
https://www.ncbi.nlm.nih.gov/pubmed/34640463
http://dx.doi.org/10.3390/jcm10194445

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