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Concept information

Preferred term

Hereditary Sensory and Motor Neuropathy  

Type

  • Topical Descriptor

Entry terms

  • Herditary Sensory and Motor Neuropathy
  • Hereditary Motor and Sensory Neuropathies
  • Hereditary Motor and Sensory Neuropathy
  • HMSN
  • Neuropathies, Hereditary Motor and Sensory

Note

  • do not confuse with HEREDITARY SENSORY AND AUTONOMIC NEUROPATHIES

Scope note

  • A group of slowly progressive inherited disorders affecting motor and sensory peripheral nerves. Subtypes include HMSNs I-VII. HMSN I and II both refer to CHARCOT-MARIE-TOOTH DISEASE. HMSN III refers to hypertrophic neuropathy of infancy. HMSN IV refers to REFSUM DISEASE. HMSN V refers to a condition marked by a hereditary motor and sensory neuropathy associated with spastic paraplegia (see SPASTIC PARAPLEGIA, HEREDITARY). HMSN VI refers to HMSN associated with an inherited optic atrophy (OPTIC ATROPHIES, HEREDITARY), and HMSN VII refers to HMSN associated with retinitis pigmentosa. (From Adams et al., Principles of Neurology, 6th ed, p1343)

History note

  • 2000(1989)

In other languages

  • Finnish

  • hereditaariset motoriset ja sensoriset neuropatiat
  • hereditääriset motoriset ja sensoriset neuropatiat
  • perinnöllinen sensorinen ja motorinen neuropatia
  • periytyvät motoriset ja sensoriset neuropatiat
  • Swedish

  • Charcot-Marie-Tooths sjukdom typ 3
  • Dejerine-Sottas neuropati
  • Dejerine-Sottas sjukdom
  • Hereditär motorisk och sensorisk neuropati, typ VII
  • Ärftlig sensorisk och motorisk neuropati

URI

http://www.yso.fi/onto/mesh/D015417

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