Respiratory Dysfunction in Children and Adolescents with Mucopolysaccharidosis Types I, II, IVA, and VI

Mucopolysaccharidosis (MPS) is a rare genetic disease involving active storage of glycosaminoglycans (GAGs). Accumulation of GAGs in the connective tissues of airways leads to progressive pulmonary dysfunction. Studies conducted in Taiwan revealed mainly restrictive pulmonary dysfunction, whereas th...

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Detalles Bibliográficos
Autores principales: Tulebayeva, Assel, Sharipova, Maira, Boranbayeva, Riza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7168931/
https://www.ncbi.nlm.nih.gov/pubmed/31991612
http://dx.doi.org/10.3390/diagnostics10020063

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7168931/
https://www.ncbi.nlm.nih.gov/pubmed/31991612
http://dx.doi.org/10.3390/diagnostics10020063

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