Myasthenic Syndrome, Congenital, 10 (CMS10)

Myasthenic Syndrome, Congenital, 10, also known as congenital myasthenic syndrome 10, is related to myasthenic syndrome, congenital, 1b, fast-channel and congenital myasthenic syndrome, and has symptoms including facial paresis An important gene associated with Myasthenic Syndrome, Congenital, 10 is DOK7 (Docking Protein 7). Affiliated tissues include brain and eye, and related phenotypes are decreased fetal movement and ophthalmoparesis