Toggle Main Menu Toggle Search

Open Access padlockePrints

The Increasing Genetic and Phenotypical Diversity of Congenital Myasthenic Syndromes

Lookup NU author(s): Dr Grace McMacken, Dr Teresinha Evangelista, Dr Sally Spendiff, Professor Hanns Lochmuller


Full text for this publication is not currently held within this repository. Alternative links are provided below where available.


Copyright © 2017, Georg Thieme Verlag KG. All rights reserved. The congenital myasthenic syndromes (CMS) are a diverse group of diseases, which result in an increasing range of phenotypes, but which are all due to inherited defects at the neuromuscular junction (NMJ). Although some patients remain genetically undiagnosed, our ability to identify the causative genes has shed new light on the role of previous uncharacterized proteins at the NMJ. Securing the genetic diagnosis can be challenging, but it is of critical importance to allow rational therapeutic intervention. In this review, we summarize the key clinical and pathologic features of the CMS subtypes, outline diagnostic clues, and challenges, and describe the recent advances that have highlighted the overlap between CMS and the muscular dystrophies and peripheral neuropathies.

Publication metadata

Author(s): McMacken G, Abicht A, Evangelista T, Spendiff S, Lochmüller H

Publication type: Article

Publication status: Published

Journal: Neuropediatrics

Year: 2017

Volume: 48

Issue: 4

Pages: 294-308

Online publication date: 15/05/2017

Acceptance date: 23/03/2017

ISSN (print): 0174-304X

ISSN (electronic): 1439-1899

Publisher: Hippokrates Verlag GmbH


DOI: 10.1055/s-0037-1602832


Altmetrics provided by Altmetric