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Congenital myasthenic syndrome 12

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Description

Congenital myasthenic syndrome-12 is an autosomal recessive neuromuscular disorder characterized by onset of proximal muscle weakness in the first decade. EMG classically shows a decremental response to repeated nerve stimulation. Affected individuals show a favorable response to acetylcholinesterase (AChE) inhibitors (summary by Senderek et al., 2011). For a discussion of genetic heterogeneity of CMS, see CMS1A (601462).

OMIM

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

238

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Genes

External Links

  • OMIM

    610542

  • Orphanet
  • HPO
  • Medgen

    C3552335

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