Genetics in Movement Disorders in Asia

Introduction

Genetics in Movement Disorders in Asia

Course Format

Live Online

Start Date

Sat, Aug 1, 2026

End Date

Sun, Aug 2, 2026

Program Description

The Genetics in Movement Disorders in Asia course is a two-day intensive online course that provides a comprehensive overview of the rapidly evolving field of genetics within movement disorders. Participants will explore the clinical application of ACMG guidelines and the interpretation of complex genetic reports alongside deep dives into the genetic foundations of Parkinson’s disease, atypical parkinsonism, dystonia, chorea, and ataxia. The program further addresses specialized topics such as mitochondrial disorders, epilepsy dyskinesia syndromes, and the critical role of genetic counseling in clinical practice, concluding with a "Case Parade" to apply theoretical knowledge to real-world scenarios.

REGISTRATION DEADLINE: July 28, 2026

Registration Type		Member Fee	Non-Member Fee
	Course Registration	N/A	$50.00

Contact Us

MDS Education
education@movementdisorders.org

Course Overview (Fees, Schedule, & Course Details)

Course Schedule Course Faculty

Schedule as of April 29, 2026

REGISTRATION FEES
MDS Members: $0 USD
Non-Members: $50 USD
*Non-members wishing to apply for MDS Membership to receive the MDS Member rate for this course will need to apply for membership no later than 2 weeks in advance of the close of registration.

Saturday, August 1, 2026 – Sunday, August 2, 2026

Day 1: Saturday, August 1, 2026 | 08:00 – 11:25 (IST)

Day 2: Sunday, August 2, 2026 | 08:00 – 11:30 (IST)

To convert to your local time, please click here: https://www.timeanddate.com/worldclock/converter.html

LEARNING OBJECTIVES

1. Evaluate genetic reports using current ACMG guidelines to determine the clinical significance of identified variants.

2. Differentiate between the genetic architectures of common and rare movement disorders, such as Parkinson’s disease versus atypical parkinsonism or chorea.

3. Identify the clinical presentations of newer repeat expansion disorders and mitochondrial movement disorders to guide targeted testing.

4. Integrate genetic counseling principles into the diagnostic workflow to support patient and family decision-making.

INTENDED AUDIENCE

This activity is intended for clinicians, fellows, neurology residents, researchers, medical students, allied health professionals, and researchers.