Harvard Catalyst Profiles

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Sturge-Weber Syndrome

"Sturge-Weber 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.

A non-inherited congenital condition with vascular and neurological abnormalities. It is characterized by facial vascular nevi (PORT-WINE STAIN), and capillary angiomatosis of intracranial membranes (MENINGES; CHOROID). Neurological features include EPILEPSY; cognitive deficits; GLAUCOMA; and visual defects.


This graph shows the total number of publications written about "Sturge-Weber Syndrome" by people in Harvard Catalyst Profiles by year, and whether "Sturge-Weber Syndrome" was a major or minor topic of these publication.
Bar chart showing 31 publications over 14 distinct years, with a maximum of 5 publications in 2013
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.