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Up to: Postsynaptic congenital myasthenic syndrome
Congenital myasthenic syndrome 3C
A congenital myasthenic syndrome characterized by autosomal recessive inheritance of postsynaptic neuromuscular junction defects, low amplitude of the miniature endplate potential and current, and early-onset muscle weakness that has material basis in compound heterozygous mutation in the CHRND gene on chromosome 2q37.
This condition has no sub-types.