Harvard Catalyst Profiles

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Usher Syndromes

"Usher Syndromes" 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.

Autosomal recessive hereditary disorders characterized by congenital SENSORINEURAL HEARING LOSS and RETINITIS PIGMENTOSA. Genetically and symptomatically heterogeneous, clinical classes include type I, type II, and type III. Their severity, age of onset of retinitis pigmentosa and the degree of vestibular dysfunction are variable.


This graph shows the total number of publications written about "Usher Syndromes" by people in Harvard Catalyst Profiles by year, and whether "Usher Syndromes" was a major or minor topic of these publication.
Bar chart showing 20 publications over 13 distinct years, with a maximum of 3 publications in 2011
To see the data from this visualization as text, click here.
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.