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Spinal Muscular Atrophies of Childhood

"Spinal Muscular Atrophies of Childhood" 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.

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A group of recessively inherited diseases that feature progressive muscular atrophy and hypotonia. They are classified as type I (Werdnig-Hoffman disease), type II (intermediate form), and type III (Kugelberg-Welander disease). Type I is fatal in infancy, type II has a late infantile onset and is associated with survival into the second or third decade. Type III has its onset in childhood, and is slowly progressive. (J Med Genet 1996 Apr:33(4):281-3)


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This graph shows the total number of publications written about "Spinal Muscular Atrophies of Childhood" by people in UAMS Profiles by year, and whether "Spinal Muscular Atrophies of Childhood" was a major or minor topic of these publications.
Bar chart showing 4 publications over 2 distinct years, with a maximum of 3 publications in 2020
To see the data from this visualization as text, click here.