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Mucopolysaccharidoses (MPSs) Highlights from WORLDSymposium 2020

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Overview / Abstract:

At WORLDSymposium 2020, new information and data were presented on Mucopolysaccharidoses (MPSs), a group of genetic lysosomal disorders. This CME activity highlights the latest information about MPSs from WORLDSymposium and provides expert analysis of its clinical relevance for busy members of the care team in order to help them care for patients with these rare diseases.

Expiration

May 01, 2021

Discipline(s)

Nurse Practitioner , Nursing CNE, Physical Therapy CE, Physician CME, Physician Assistant CME

Format

Webinar / Webcast / Video

Credits / Hours

.25

Accreditation

ACCME

Presenters / Authors / Faculty

Barbara K. Burton, MD
Attending Physician, Genetics, Birth Defects & Metabolism
Ann & Robert H. Lurie Children’s Hospital of Chicago
Professor of Pediatrics
Northwestern University Feinberg School of Medicine
Chicago, IL

Activity Specialities / Related Topics

Primary Care, Pediatrics, Osteopathy / Osteopathic Medicine , Neurology, Internal Medicine, Hematology, Genetics, Gastroenterology / GI, Education / Teaching

Sponsors / Supporters / Grant Providers

Ultragenyx Pharmaceutical Inc.

Keywords / Search Terms

CheckRare Mucopolysaccharidoses, MPS, inherited metabolic disease, rare disease, MPS IIIA, heparan N-sulfatase MPS IIIB, alpha-N-acetylglucosaminidase MPS IIIC, acetyl-CoA:alpha-glucosaminide acetyltransferase, MPS IIID, Hurler Syndrome, Hurler-Scheie Syndrome, Scheie Syndrome, Hunter Syndrome, Sanfilippo Syndrome, Morquio Syndrome, Maroteaux-Lamy Syndrome, Sly Syndrome, lysosomal storage disorder, Barbara Burton MD, WORLDSYM

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