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Mucopolysaccharidosis I

Overview / Abstract:	Early symptoms for Mucopolysaccharidosis I (MPS I), especially in those with the attenuated form of the disease, can be very difficult to distinguish from other more common conditions. Since this progressive disease has a treatment that can slow progression, it is imperative that clinicians recognize symptoms early so a correct diagnosis can be made. In this module, our faculty educator will explore making a proper diagnosis of MPS I.
Expiration	Jul 31, 2021
Format	Webinar / Webcast / Video
Credits / Hours	1.0
Accreditation	American Academy of CME, Inc.
Presenters / Authors / Faculty	Paul Orchard, MD Medical Director Inherited Metabolic and Storage Disease Program Professor of Pediatrics Division of Blood and Marrow Transplantation University of Minnesota Medical School
Sponsors / Supporters / Grant Providers	Sanofi Genzyme
Keywords / Search Terms	CheckRare Mucopolysaccharidosis I, MPS I, MPS 1, Paul Orchard MD, lysosomal storage disease, rare disease, rare disorder, gaucher, Fabry, Pompe, Free CE CME

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