Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Postsynaptic congenital myasthenic syndrome
Congenital myasthenic syndrome 3B
A congenital myasthenic syndrome characterized by autosomal recessive inheritance of postsynaptic neuromuscular junction defects resulting in rapid decay in endplate current and a failure to reach the threshold for depolarization and early onset progressive muscular weakness that has material basis in homozygous or compound heterozygous mutation in the CHRND gene on chromosome 2q37.
This condition has no sub-types.