Neuropathies

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  • Spinal Muscular Atrophy (SMA) and related syndromes:
    • Infantile spinal muscular atrophy, type I [Werdnig-Hoffman] 
    • Other inherited spinal muscular atrophy
    • Progressive bulbar palsy of childhood [Fazio-Londe]
    • SMA adult form
    • SMA childhood form, type II
    • Distal SMA
    • SMA juvenile form, type III [Kugelberg-Welander]
    • SMA scapuloperoneal form
  • Systemic atrophies primarily affecting central nervous system in diseases classified elsewhere 
  • Primary disorders of muscles 
  • Paraneoplastic and neuropathy
    • Sensorial paraneoplastic neuropathy [Denny Brown] 
  • Hereditary motor and sensory neuropathy
    • Charcot-Marie-Tooth
    • Déjerine-Sottas
    • Refsum's disease 
    • Hereditary motor and sensory neuropathy, types I-IV
    • Hypertrophic neuropathy of infancy
    • Peroneal muscular atrophy (axonal type) (hypertrophic type)
    • Roussy-Lévy syndrome
  • Neuropathy in association with hereditary ataxia , such as fredrich’s ataxia or Ataxia Telangectasia
  • Idiopathic progressive neuropathy
  • Inflammatory polyneuropathy
    • Guillain-Barré syndrome 
    • Acute (post-) infective polyneuritis
  • Drug-induced/Alcoholic/Toxic Agent/Radiation induced polyneuropathy 
  • Serum neuropathy 
  • Polyneuropathy in infectious and parasitic diseases classified elsewhere:
    • diphtheria 
    • infectious mononucleosis         
    • leprosy
    • Lyme disease
    • mumps
    • postherpetic
    • syphilis, late
    • congenital syphilis, late
    • tuberculous
    • Diabetic polyneuropathy
  • Polyneuropathy in:
    • other endocrine and metabolic diseases   
    • neoplastic disease
    •  nutritional deficiency
    • systemic connective tissue disorders
    • other musculoskeletal disorders
    • Uraemic neuropathy  

INCLUDES:  arthrogryposis multiplex congenita, metabolic myopathies

EXCLUDES: Dermatomyositis