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Slowly progressive distal muscle weakness: neuropathy or myopathy?

Yafit NahariAhmed AbbasElizabeth CurtisSaiju Jacob
Published in: BMJ case reports (2019)
Nonaka myopathy is an autosomal recessive and slowly progressive distal myopathy. It is part of a rare group of myopathies predominantly affecting the distal limb musculature. Over 150 cases have been reported across the Middle East, Japan and Europe. We report the case of a 33-year-old woman presenting with symmetrical upper and lower limb weakness, most severely affecting the distal muscle groups. After extensive neurological investigation including neurophysiology, muscle biopsy and genetic analysis, she was finally diagnosed with Nonaka myopathy and treated conservatively with physiotherapy.
Keyphrases
  • late onset
  • lower limb
  • muscular dystrophy
  • minimally invasive
  • skeletal muscle
  • multiple sclerosis
  • early onset
  • case report
  • ultrasound guided
  • african american
  • blood brain barrier