CMS (Congenital Myasthenic Syndrome)
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Congenital Myasthenic Syndrome (CMS) includes a group of rare, inherited neuromuscular disorders. Inherited genetic faults cause CMS rather than an autoimmune response.
These genetic changes severely disrupt communication between nerves and muscles. Symptoms typically begin during infancy or early childhood. Patients commonly experience profound muscle weakness, general fatigue, and difficulty with voluntary movement.
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