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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Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: Springer Netherlands 2011
Matèries:
Review
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3228957/
https://ncbi.nlm.nih.gov/pubmed/21744090
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10545-011-9359-8
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