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This course will provide a summary of the most common clinical presentations of Parkinson’s disease, Essential Tremor, and Multiple Sclerosis. Strategies for efficient differential diagnosis of each disease will be reviewed. Existing or emerging biomarkers will be discussed. Finally, the talk will conclude with a brief outline of general treatment strategies and emerging trends and how to proceed if uncertainty remains in the differential diagnosis.
This activity is supported by an educational grant from AbbVie.
While the number of people affected by an individual rare disease may be small, the total number of people with a rare diseases—an estimated 25 to 30 million in the United States—is enormous!
What is Pompe disease?
It is a glycogen storage disease type II and considered to be a rare inherited autosomal recessive disorder caused by mutations in the gene that encodes for acid alpha-glucosidase (GAA).
This activity is supported by an educational grant from Spark Therapeutics. This activity is supported by an educational grant from AbbVie.
These activities are provided by Global Education Group.
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