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Charcot-Marie-Tooth Disease

"Charcot-Marie-Tooth Disease" 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 hereditary motor and sensory neuropathy transmitted most often as an autosomal dominant trait and characterized by progressive distal wasting and loss of reflexes in the muscles of the legs (and occasionally involving the arms). Onset is usually in the second to fourth decade of life. This condition has been divided into two subtypes, hereditary motor and sensory neuropathy (HMSN) types I and II. HMSN I is associated with abnormal nerve conduction velocities and nerve hypertrophy, features not seen in HMSN II. (Adams et al., Principles of Neurology, 6th ed, p1343)


publications
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This graph shows the total number of publications written about "Charcot-Marie-Tooth Disease" by people in Harvard Catalyst Profiles by year, and whether "Charcot-Marie-Tooth Disease" was a major or minor topic of these publication.
Bar chart showing 63 publications over 27 distinct years, with a maximum of 6 publications in 2019
To see the data from this visualization as text, click here.
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