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.

About CMS

An overview of Congenital Myasthenic Syndromes - how it is caused, how it is inherited, and what its symptoms are

Patient organizations

Patient organizations and advocacy groups providing support for patients with CMS


Patient Registries

Find out about various patient registries for CMS

Meetings and Events

Any meetings or conferences that are relevant to CMS will be available in this section

12 Apr 2017