Harvard Catalyst Profiles

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Corneal Dystrophies, Hereditary

"Corneal Dystrophies, Hereditary" 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.

Bilateral hereditary disorders of the cornea, usually autosomal dominant, which may be present at birth but more frequently develop during adolescence and progress slowly throughout life. Central macular dystrophy is transmitted as an autosomal recessive defect.


This graph shows the total number of publications written about "Corneal Dystrophies, Hereditary" by people in Harvard Catalyst Profiles by year, and whether "Corneal Dystrophies, Hereditary" was a major or minor topic of these publication.
Bar chart showing 28 publications over 17 distinct years, with a maximum of 3 publications in 2007 and 2013 and 2016
To see the data from this visualization as text, click here.
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Funded by the NIH/NCATS Clinical and Translational Science Award (CTSA) program, grant number UL1TR001102, and through institutional support from Harvard University, Harvard Medical School, Harvard T.H. Chan School of Public Health, Beth Israel Deaconess Medical Center, Boston Children's Hospital, Brigham and Women's Hospital, Massachusetts General Hospital and the Dana Farber Cancer Institute.