Critical clinical situations in adult patients with Mucopolysaccharidoses (MPS)

BACKGROUND: Mucopolysaccharidoses (MPS) are rare, inherited disorders associated with enzyme deficiencies that result in glycosaminoglycan (GAG) accumulation in multiple organ systems. Management of MPS is evolving as patients increasingly survive to adulthood and undergo multiple surgeries througho...

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Detalles Bibliográficos
Autores principales: Stepien, Karolina M., Gevorkyan, Anait K., Hendriksz, Christian J., Lobzhanidze, Tinatin V., Pérez-López, Jordi, Tol, Govind, del Toro Riera, Mireia, Vashakmadze, Nato D., Lampe, Christina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7227065/
https://www.ncbi.nlm.nih.gov/pubmed/32410642
http://dx.doi.org/10.1186/s13023-020-01382-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7227065/
https://www.ncbi.nlm.nih.gov/pubmed/32410642
http://dx.doi.org/10.1186/s13023-020-01382-z

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