Congenital Myasthenic Syndrome by Mutation of the ColQ Gene: Phenotypic and Evolutionary Profile of Three Algerian Families

Background. - Congenital myasthenic syndromes (CMS) are rare genetic neuromuscular disorders. The COLQ gene encoding the collagenous subunit of the acetyl cholinesterase enzyme tail is implicated in a synaptic form of CMS (also called type 5, according to the new gene table 2020 classification). Objective. - To study the clinical phenotype of three families with COLQ gene mutations. Methods. - We report a series of three consanguineous families, with seven affected patients, carrying three different mutations of the COLQ gene, one of which has never been reported in the literature before. Results. - We studied their clinical and paraclinical phenotypes, and try to compare the three families as well as compare them with other series carrying COLQ gene mutations reported in the literature. Conclusion. - COLQ gene mutations have phenotypic particularities that must be recognized to propose appropriate genetic study. & COPY; 2023 Elsevier Masson SAS. All rights reserved.