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Hereditary Sensory and Motor Neuropathy

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)

Year introduced: 2000(1989)

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Subheadings:

Tree Number(s): C10.500.300, C10.574.500.495, C10.668.829.800.300, C16.131.666.300, C16.320.400.375

MeSH Unique ID: D015417

Entry Terms:

  • Neuropathies, Hereditary Motor and Sensory
  • Hereditary Motor and Sensory Neuropathy
  • HMSN
  • Herditary Sensory and Motor Neuropathy
  • Hereditary Motor and Sensory Neuropathies
  • Hereditary, Type VII, Motor and Sensory Neuropathy
  • HMSN Type VII
  • HMSN Type VIIs
  • Type VII, HMSN
  • HMSN Type III
  • HMSN Type IIIs
  • Charcot-Marie-Tooth Disease, Type 3
  • Charcot Marie Tooth Disease, Type 3
  • CMT4f
  • Dejerine-Sottas Disease
  • Dejerine Sottas Disease
  • Disease, Dejerine-Sottas
  • Dejerine-Sottas Neuropathy
  • Dejerine Sottas Neuropathy
  • Neuropathy, Dejerine-Sottas
  • Hereditary, Type III, Motor and Sensory Neuropathy
  • HMSN3
  • Hereditary Motor and Sensory Neuropathy 3
  • Hypertrophic Neuropathy of Dejerine-Sottas
  • Dejerine-Sottas Hypertrophic Neuropathy
  • Hypertrophic Neuropathy of Dejerine Sottas
  • Hereditary Motor and Sensory Neuropathy Type III
  • Charcot-Marie-Tooth Disease, Demyelinating, Type 4f
  • Dejerine-Sottas Syndrome
  • Dejerine Sottas Syndrome
  • Syndrome, Dejerine-Sottas

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