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Asymmetric Myopathic Weakness

• Hereditary myopathies
  • Facioscapulohumeral Dystrophy
  • McLeod Syndrome
  • Glycogen storage disorders: Some patients
    • Phosphorylase deficiency (McArdle's)
    • Acid maltase deficiency (Adult onset)
  • Neutral lipid storage disease
  • Distal myopathy
    • Atypical Miyoshi: Dysferlin
    • Vocal cord & Pharyngeal: Matrin 3
    • MPD3
    • MPD4: Filamin C
    • MSP4: SQSTM1
  • LGD
    • 1C: Caveolin-3
    • 2A: Calpain-3
    • 2B (Miyoshi myopathy): Dysferlin
    • 2I: FKRP
    • 2L: Anoctamin 5
    • Dystrophinopathy: Female carriers
  • Other myopathies
    • Reducing body myopathy: FHL1
    • IBMPFD: VCP
    • ACTA1 rod myopathy: Mosaic (de novo) mutation
  • Carriers, Manifesting female
    • Dystrophinopathy
    • Centronuclear myopathy
• Acquired & sporadic myopathies
  • Myositis
    • IM-VAMP: Inclusion Body
    • Focal: Orbital; Quadriceps
  • Myasthenia Gravis: Cranial nerve musculature
• Also see: Neuropathies, Asymmetric