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Hereditary Sensory and Motor Neuropathy
Definition: 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 HMSN I. HMSN VII refers to hypertrophic neuropathy of infancy. HMSN VII refers to REFSUM DISEASE. HMSN VII refers to a condition marked by a hereditary motor and sensory neuropathy associated with spastic paraplegia (see SPASTIC PARAPLEGIA, HEREDITARY). HMSN VII 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)

Synonym(s): Dejerine-Sottas Disease / HMSN / HMSN Type III / HMSN Type VII / Hereditary Motor and Sensory Neuropathies / Hereditary, Type III, Motor and Sensory Neuropathy / Hereditary, Type VII, Motor and Sensory Neuropathy / Neuropathies, Hereditary Motor and Sensory / Herditary Sensory and Motor Neuropathy / Dejerine Sottas Disease / Disease, Dejerine-Sottas / HMSN Type IIIs / HMSN Type VIIs / Type VII, HMSN

Narrow term(s):
   Alstrom Syndrome    Charcot-Marie-Tooth Disease    Giant Axonal Neuropathy
   Refsum Disease    Spastic Paraplegia, Hereditary

MeSH 2010 © U.S. National Library of Medicine®.
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  Web resources for "Hereditary Sensory and Motor Neuropathy"
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view the HON description of the site HONcode - D Trisomy Syndrome - Dejerine Sottas Disease - D - Health Center - Everyday Health - EverydayHealth.com www.everydayhealth.com  
view the robot description of the site rare-diseases — National Organization for Rare Disorderswww.rarediseases.org  
view the HON description of the site HONcode - Patients on Youtube, movies - Neuropathiewww.neuropathie.nu 2
view the robot description of the site Whonamedit - Charcot-Marie-Tooth diseasewww.whonamedit.com  
view the HON description of the site HONcode - CMT United Kingdom - Introducing CMT United Kingdomwww.cmt.org.uk  
view the HON description of the site HONcode - Types of Peripheral Neuropathy - Hereditary - Charcot-Marie-Tooth Disease (CMT) millercenter.uchicago.edu  
view the HON description of the site HONcode - Types of Peripheral Neuropathy - Hereditary - Charcot-Marie-Tooth Disease (CMT) peripheralneuropathycenter.uchicago.edu  
view the HON description of the site HONcode - EuroGentest: Clinical Utility Gene Cardswww.eurogentest.org  
 
 
Broader term(s): - Nervous System Malformations - Nervous System Diseases - Neurodegenerative Diseases - Polyneuropathies - Peripheral Nervous System Diseases - Neuromuscular Diseases
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Broader term(s): - Nervous System Diseases
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Broader term(s): - Nervous System Diseases

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Broader term(s): - Neurodegenerative Diseases

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  Broader term(s):
      Diseases
          Congenital, Hereditary, and Neonatal Diseases and Abnormalities
              Genetic Diseases, Inborn
                  Heredodegenerative Disorders, Nervous System 
              Congenital Abnormalities
                  Nervous System Malformations 
      Diseases
          Nervous System Diseases
              Neuromuscular Diseases
                  Peripheral Nervous System Diseases
                      Polyneuropathies 
              Neurodegenerative Diseases
                  Heredodegenerative Disorders, Nervous System 
              Nervous System Malformations 

MeSH 2010 © U.S. National Library of Medicine®.

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