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Hereditary Sensory and Autonomic Neuropathies

"Hereditary Sensory and Autonomic Neuropathies" 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 inherited disorders characterized by degeneration of dorsal root and autonomic ganglion cells, and clinically by loss of sensation and autonomic dysfunction. There are five subtypes. Type I features autosomal dominant inheritance and distal sensory involvement. Type II is characterized by autosomal inheritance and distal and proximal sensory loss. Type III is DYSAUTONOMIA, FAMILIAL. Type IV features insensitivity to pain, heat intolerance, and mental deficiency. Type V is characterized by a selective loss of pain with intact light touch and vibratory sensation. (From Joynt, Clinical Neurology, 1995, Ch51, pp142-4)


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This graph shows the total number of publications written about "Hereditary Sensory and Autonomic Neuropathies" by people in Harvard Catalyst Profiles by year, and whether "Hereditary Sensory and Autonomic Neuropathies" was a major or minor topic of these publication.
Bar chart showing 19 publications over 12 distinct years, with a maximum of 3 publications in 2019
To see the data from this visualization as text, click here.
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