Cardiac disease in patients with mucopolysaccharidosis: presentation, diagnosis and management

The mucopolysaccharidoses (MPSs) are inherited lysosomal storage disorders caused by the absence of functional enzymes that contribute to the degradation of glycosaminoglycans (GAGs). The progressive systemic deposition of GAGs results in multi-organ system dysfunction that varies with the particula...

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Detalles Bibliográficos
Autores principales: Braunlin, Elizabeth A., Harmatz, Paul R., Scarpa, Maurizio, Furlanetto, Beatriz, Kampmann, Christoph, Loehr, James P., Ponder, Katherine P., Roberts, William C., Rosenfeld, Howard M., Giugliani, Roberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2011
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3228957/
https://www.ncbi.nlm.nih.gov/pubmed/21744090
http://dx.doi.org/10.1007/s10545-011-9359-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3228957/
https://www.ncbi.nlm.nih.gov/pubmed/21744090
http://dx.doi.org/10.1007/s10545-011-9359-8

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