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C192 - Paroxysmal Movement Disorders

Event Time: Thursday April 27, 2017 7:00 am to 9:00 am
Topic(s): Movement Disorders
Director(s): Kailash Bhatia MD, FAAN
Description: Advances in identification of different forms of paroxysmal movement disorders and also molecular genetics have greatly impacted the practice of clinicians dealing with these conditions. Through presentations of video cases of common and rarer forms of acquired and genetic paroxysmal movement disorders the faculty will facilitate a discussion about differential diagnosis and laboratory evaluation. Each case will be followed by an overview and update on the topic.
Completion Message: Participants should be able to identify the different forms pf paroxysmal movement disorders and be able to order appropriate investigations, whether they be imaging, biochemical, CSF examination, or genetics to arrive at the right diagnosis; and consider the appropriate drug or other management for each form of paroxysmal movement disorder.
CME Credits: 2
Core Competencies: Medical Knowledge, Patient Care

Program Speakers - Tentative

Start/End Time Title Faculty
7:00 AM - 8:00 AM Primary Paroxysmal Dyskinesias Kailash Bhatia MD, FAAN 
8:00 AM - 9:00 AM Secondary Paroxysmal Dyskinesias Kapil Sethi MD, FRCP (UK), FAAN 

Disclosures

Speaker Disclosure
Kailash P. Bhatia, MD, FAAN Dr. Bhatia has nothing to disclose.

Kapil D. Sethi, MD, FRCP (UK), FAAN Dr. Sethi has received personal compensation for consulting, serving on a scientific advisory board, speaking, or other activities with Neurocrine,ADAMAS,Merz,Synuvion.

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