Muscular channelopathy

Part of

Sub-types of Muscular channelopathy

• Thomsen and Becker disease 9 trials
  2 sub-types

  • Myotonia congenita, autosomal dominant 0 trials
  • Myotonia congenita, autosomal recessive 0 trials
• RYR1-related myopathy 5 trials · 6 incl. sub-types
  5 sub-types

  • Central core myopathy 2 trials
  • King-Denborough syndrome 0 trials
  • Congenital multicore myopathy with external ophthalmoplegia 0 trials
  • Congenital myopathy with myasthenic-like onset 0 trials
  • Rhabdomyolysis-myalgia syndrome 0 trials
• Malignant hyperthermia of anesthesia 5 trials
• SCN4A-related channelopathy 1 trial · 2 incl. sub-types
  4 sub-types

  • Hyperkalemic periodic paralysis 1 trial
  • Paramyotonia congenita of Von Eulenburg 1 trial
  • Hypokalemic periodic paralysis, type 2 0 trials
  • Potassium-aggravated myotonia 0 trials Sub-types →
• Andersen-Tawil syndrome 0 trials
• CNGB3-related retinopathy 0 trials
  1 sub-type

  • Achromatopsia 3 0 trials
• Isaac syndrome 0 trials
• Morvan syndrome 0 trials
• Neurological muscular channelopathy due to a genetic calcium channel defect 0 trials
• Neurological muscular channelopathy due to a genetic chloride channel defect 0 trials
• Neurological muscular channelopathy due to a genetic potassium channel defect 0 trials
• Neurological muscular channelopathy due to a genetic sodium channel defect 0 trials