To report SUSPECTED ADVERSE REACTIONS, contact argenx at 1-833-argx411 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch

Argenx

To report SUSPECTED ADVERSE REACTIONS, 
contact argenx at 1-833-argx411 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch

Educational Events

Educational events providing practical guidance to support timely suspicion and diagnosis of CMS

Webinar: Diagnosing Congenital Myasthenic Syndromes

Congenital myasthenic syndromes (CMS) are the masters of disguise, and diagnosis can be challenging. 

Join one of our complimentary interactive webinars, which combine expert-led presentations with real-world case-based discussion to help provide clear, practical guidance on the timely recognition and diagnosis of CMS.

By the end of these expert-led webinars, you will understand:

  • Key signs and symptoms that may raise suspicion of CMS, and the associated patient burden​
  • Clinical features that may help distinguish CMS from other neuromuscular disorders​
  • How to access free genetic testing and refer patients to CMS specialists
  • Available patient support resources and current clinical trial opportunities
Diagnosing Congenital Myasthenic Syndromes (CMS)
Diagnosing Congenital Myasthenic Syndromes (CMS)
Wednesday, October 7

12pm–1pm EDT​​

Faculty: Dr. Partha Ghosh, MD.​

Dr. Ghosh is based at Boston Children's Hospital and holds the following clinical and academic roles:

  • Neurologist, Department of Neurology
  • Director, EMG laboratory
  • Director, Muscular Dystrophy Association Care Center
  • Associate Professor of Neurology, Harvard Medical School​
Diagnosing Congenital Myasthenic Syndromes (CMS)
Thursday, October 29

12pm–1pm EDT​

Faculty: Dr. Miriam Freimer, MD.​​

Dr. Freimer is based at Wexner Medical Center, Ohio center and​ holds the following clinical and ​academic roles:​

  • Physician, Department of Neurology
  • Director, Division of Neuromuscular Disorders​
  • Director, EMG laboratory
  • Co-Director, Myasthenia Gravis Clinic
  • Professor of Neurology, Ohio State University Wexner Medical Center​
Diagnosing Congenital Myasthenic Syndromes (CMS)
Monday, November 16
12pm–1pm CST

Faculty: Dr. Nancy Kuntz, MD.​

Dr. Kuntz is based at Ann and Robert H Lurie Children's Hospital of Chicago and holds the following clinical and academic roles:​

  • Physician, Division of Neurology​
  • Medical Director, Mazza Foundation Neuromuscular Program​
  • Director, Muscular Dystrophy Association Care Center​
  • Professor of Pediatrics and Neurology, Northwestern University Feinberg ​School of Medicine​

For US healthcare professionals only.​
These events are not accredited for Continuing Medical Education (CME) credit.
Sponsored by argenx.

Get in touch with our Medical team

If you are unable to attend any of the live events listed, or would prefer a 1:1 discussion on CMS, please click the button below to arrange a meeting with your local argenx Medical team

Diagnosing Congenital Myasthenic Syndromes (CMS)

Coming soon!

A recording of a previous event will be available soon

If it could be CMS, order a free genetic test to diagnose, or refer to a specialist for support
If it is CMS, consider referring your patient for enrollment into a clinical study to improve understanding of the disease

Learn more:

Free genetic testing
Referring to a specialist
Diagnosing CMS
CMS clinical studies

Additional CMS information

Diagnosis and referral resources

Explore CMS diagnosis, specialist support options, and current research opportunities to help improve outcomes for people living with CMS

Overview

Explore an overview of CMS, their key clinical features, and common misdiagnoses