Definitions for wolfram syndrome
This page provides all possible meanings and translations of the word wolfram syndrome
Wolfram syndrome, also called DIDMOAD, is a rare genetic disorder, causing diabetes mellitus, optic atrophy, and deafness as well as various other possible disorders. It was first described in four siblings in 1938 by Dr. Don J. Wolfram, M.D. The disease affects the brain and central nervous system.
U.S. National Library of Medicine
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.
Find a translation for the wolfram syndrome definition in other languages:
Select another language:
Discuss these wolfram syndrome definitions with the community:
Use the citation below to add this definition to your bibliography:
"wolfram syndrome." Definitions.net. STANDS4 LLC, 2014. Web. 23 Apr. 2014. <http://www.definitions.net/definition/wolfram syndrome>.