Harvard Catalyst Profiles

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

Wolfram Syndrome

"Wolfram 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 hereditary condition characterized by multiple symptoms including those of DIABETES INSIPIDUS; DIABETES MELLITUS; OPTIC ATROPHY; and DEAFNESS. This syndrome is also known as DIDMOAD (first letter of each word) and is usually associated with VASOPRESSIN deficiency. It is caused by mutations in gene WFS1 encoding wolframin, a 100-kDa transmembrane protein.


This graph shows the total number of publications written about "Wolfram Syndrome" by people in Harvard Catalyst Profiles by year, and whether "Wolfram Syndrome" was a major or minor topic of these publication.
Bar chart showing 7 publications over 7 distinct years, with a maximum of 1 publications in 1989 and 2003 and 2006 and 2007 and 2008 and 2012 and 2014
To see the data from this visualization as text, click here.
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.