Details
Etiopathogenesis of PD is complex and in a majority of patients, a combination of genetic and environmental factors have been postulated. Familial PD due to single gene mutation constitutes approximately 10 % of all PD cases and can be divided into autosomal dominant, autosomal recessive and high risk loci. Details of gene mutations and disorders associated with Parkinson’s Disease will be reviewed in this course.
Part of the Coffee Break CME Series. The International Parkinson and Movement Disorder Society designates this educational activity for a maximum of 2.0 AMA PRA Category 1 Credits™.
This module will take approximately 2 hours to complete.
Faculty- Dr. Anil Venkitachalam, Dr. Oksana Suchowersky