Myasthenic syndrome, congenital, 1B, fast-channel

A congenital myasthenic syndrome characterized by defects in postsynaptic neuromuscular junctions with early-onset progressive muscle weakness that has material basis in mutation in the CHRNA1 gene on chromosome 2q.

Also known as: CMS1B, congenital myasthenic syndrome type 1B, myasthenic syndrome, congenital, 1B, fast-channel, congenital myasthenic syndrome 1B, myasthenic syndrome, congenital, 1B, FAST-channel

1 clinical trial for this condition and its sub-types.