Congenital Myasthenic Syndromes overview
This section brings together information about Congenital Myasthenic Syndromes from across the website. Much of the information here is especially relevant for individuals and families affected by CMS, but family doctors and researchers should also find something of interest.
Browse through this section for specific information about CMS, and also take a look at the other areas of our website for more general information about TREAT-NMD and the resources we offer.
An overview of Congenital Myasthenic Syndromes - how it is caused, how it is inherited, and what its symptoms are
Patient organizations and advocacy groups providing support for patients with CMS
Find out about various patient registries for CMS
Any meetings or conferences that are relevant to CMS will be available in this section