Non-cardiac Manifestations in Adult Patients With Mucopolysaccharidosis

Mucopolysaccharidoses (MPS) are a heterogeneous group of disorders that results in the absence or deficiency of lysosomal enzymes, leading to an inappropriate storage of glycosaminoglycans (GAGs) in various tissues of the body such as bones, cartilage, heart valves, arteries, upper airways, cornea,...

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Detalles Bibliográficos
Autores principales: Stepien, Karolina M., Bentley, Andrew, Chen, Cliff, Dhemech, M. Wahab, Gee, Edward, Orton, Peter, Pringle, Catherine, Rajan, Jonathan, Saxena, Ankur, Tol, Govind, Gadepalli, Chaitanya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Cardiovascular Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8935042/
https://www.ncbi.nlm.nih.gov/pubmed/35321113
http://dx.doi.org/10.3389/fcvm.2022.839391

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8935042/
https://www.ncbi.nlm.nih.gov/pubmed/35321113
http://dx.doi.org/10.3389/fcvm.2022.839391

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