Harvard Catalyst Profiles

Contact, publication, and social network information about Harvard faculty and fellows.

Weill-Marchesani Syndrome

"Weill-Marchesani Syndrome" 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.

Rare congenital disorder of connective tissue characterized by brachydactyly, joint stiffness, childhood onset of ocular abnormalities (e.g., microspherophakia, ECTOPIA LENTIS; GLAUCOMA), and proportionate short stature. Cardiovascular anomalies are occasionally seen.


This graph shows the total number of publications written about "Weill-Marchesani Syndrome" by people in Harvard Catalyst Profiles by year, and whether "Weill-Marchesani Syndrome" was a major or minor topic of these publication.
Bar chart showing 3 publications over 2 distinct years, with a maximum of 2 publications in 2017
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.