231 top medical experts on Wolfram Syndrome across 31 countries and 14 U.S. states, including 64 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Wolfram Syndrome: 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.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Deaf-Blind Disorders (506), Diabetes Insipidus (1,413), Hereditary Optic Atrophies (523), Type 1 Diabetes Mellitus (5,220).
  4. Clinical Trials ClinicalTrials.gov : at least 9 including 1 Active, 1 Completed, 5 Recruiting
  5. Synonyms: DIDMOAD,  DIDMOAD Syndrome


  

        

                    


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