How is Congenital Myasthenic Syndrome (CMS) Different from Myasthenia Gravis (MG)?

RARE TIPS
Written By Know Rare Team

Get the basics about CMS, a rare genetic condition.

To get more information on clinical studies in CMS and find out how we can help, contact us.

Latest From Know Rare

Blog v2
Promising News from a Clinical Study in Becker Muscular Dystrophy
Promising News from a Clinical Study in Becker Muscular Dystrophy
Living Your Dreams When Living with Rare Disease: How Chris Anselmo Learned to Follow His Heart
Living Your Dreams When Living with Rare Disease: How Chris Anselmo Learned to Follow His Heart
Organization Spotlight: CureGRIN
Organization Spotlight: CureGRIN
Share your Rare: Edward Gent
Share your Rare: Edward Gent
Latest News in Sickle Cell Disease
Latest News in Sickle Cell Disease
Organization Spotlight: Bliss Health
Organization Spotlight: Bliss Health
Perceptions of Pain: Research Shows It’s Personal
Perceptions of Pain: Research Shows It’s Personal
Three Ways to Get Access to High Cost Treatments
Three Ways to Get Access to High Cost Treatments
Changemakers in Rare: Becca Salky
Changemakers in Rare: Becca Salky
Announcing Know Rare’s New Podcast Series: Rare Insights
Announcing Know Rare’s New Podcast Series: Rare Insights
Why Men's Health Week Matters for the Rare Community
Why Men's Health Week Matters for the Rare Community
How Know Rare is Celebrating Pride Month
How Know Rare is Celebrating Pride Month
Know Rare Connect: Living With Myositis
Know Rare Connect: Living With Myositis
Embracing Risks: How Taking Chances Enhances Life with a Rare Disease
Embracing Risks: How Taking Chances Enhances Life with a Rare Disease
Mark Your Calendar for TSF's Atlanta Patient Day
Mark Your Calendar for TSF's Atlanta Patient Day
Celebrating International Clinical Trials Day
Celebrating International Clinical Trials Day
The Surprising Link Between Exercise and Myositis
The Surprising Link Between Exercise and Myositis
On Family, Fortitude, and Forces of Nature
On Family, Fortitude, and Forces of Nature
Lindsay’s Story: What It’s Like to Live with Myositis
Lindsay’s Story: What It’s Like to Live with Myositis
May Is Myositis Awareness Month
May Is Myositis Awareness Month
The Underappreciated Art of Slowing Down
The Underappreciated Art of Slowing Down
Why 2024 Is Already an Encouraging Year for the Rare Disease Community
Why 2024 Is Already an Encouraging Year for the Rare Disease Community
Organization Spotlight: The International Waldenstrom's Macroglobulinemia Foundation (IWMF)
Organization Spotlight: The International Waldenstrom's Macroglobulinemia Foundation (IWMF)
Defining the Disease: The MOG Project
Defining the Disease: The MOG Project
Organization Spotlight: The MOG Project
Organization Spotlight: The MOG Project
How is Congenital Myasthenic Syndrome (CMS) Different from Myasthenia Gravis (MG)?
How is Congenital Myasthenic Syndrome (CMS) Different from Myasthenia Gravis (MG)?
What You Need to Know about CMS and Clinical Trials
What You Need to Know about CMS and Clinical Trials
Needle Phobia in Children: What It Is, What It Isn’t, and How to Help
Needle Phobia in Children: What It Is, What It Isn’t, and How to Help
The Link Between Oral Wellness and Your Overall Health
The Link Between Oral Wellness and Your Overall Health
All Good Things
All Good Things
Know Rare Team
Previous

Organization Spotlight: The MOG Project
Next

What You Need to Know about CMS and Clinical Trials