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Hereditary Sensory and Motor Neuropathy

"Hereditary Sensory and Motor Neuropathy" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information
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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)


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This graph shows the total number of publications written about "Hereditary Sensory and Motor Neuropathy" by people in Harvard Catalyst Profiles by year, and whether "Hereditary Sensory and Motor Neuropathy" was a major or minor topic of these publication.
Bar chart showing 13 publications over 9 distinct years, with a maximum of 3 publications in 1996 and 2019
To see the data from this visualization as text, click here.
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