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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Dades bibliogràfiques
Publicat a:Orphanet J Rare Dis
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2020
Matèries:
Research
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7227065/
https://ncbi.nlm.nih.gov/pubmed/32410642
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-020-01382-z
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