Share: Facebook Twitter LinkedIn
Activity Provided By:

CheckRare

Fabry Disease Highlights from WORLDSymposium 2020

Access Activity

Overview / Abstract:

At WORLDSymposium 2020, new information and data were presented on Fabry disease, a rare lysosomal storage disorder. This CME/CNE activity highlights the latest information about Fabry disease 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 this rare disease.

Expiration

Apr 30, 2021

Discipline(s)

Nurse Practitioner , Nursing CNE, Physician CME, Physician Assistant CME

Format

Webinar / Webcast / Video

Credits / Hours

.25

Accreditation

AACME

Presenters / Authors / Faculty

Ozlem Goker-Alpan, MD
Founder and President
Lysosomal & Rare Disorders Research & Treatment Center
Fairfax, VA

Activity Specialities / Related Topics

Pediatrics, Neurology, Internal Medicine, Hematology, Genetics, Dermatology

Sponsors / Supporters / Grant Providers

Genzyme Corporation

Keywords / Search Terms

CheckRare Fabry Disease, Genetics, Rare Disease, Ozlem Goker-Alpan MD, lysosomal storage disorder, lysosomal disease, Angiokeratoma diffuse, Anderson-Fabry disease, Hereditary dystopic lipidosis, Alpha-galactosidase A deficiency GLA deficiency, Angiokeratoma corporis diffusum, Ceramide trihexosidase deficiency, Genzyme, Sanofi, Sphingolipidosis, Lysosomal enzymes, orphan disease, orphan drug, Free CE CME

Access Activity

CORE Higher Education Group, CESearchEngine.com, and our advertising partners do not endorse and do not verify the accuracy of the content in the activities presented on the CESearchEngine.com website or within our mobile apps.CORE Higher Education Group, CESearchEngine.com, and our advertising partners are not responsible for errors, omissions, or misrepresentations contained within activities presented on the CESearchEngine website or within our mobile apps. For complete details, please read the CESearchEngine.com Terms of Service. Site Map