208 top medical experts on Lipoid Proteinosis of Urbach and Wiethe across 24 countries and 7 U.S. states, including 38 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Lipoid Proteinosis of Urbach and Wiethe: An autosomal recessive disorder characterized by glassy degenerative thickening (hyalinosis) of skin; mucosa; and certain viscera. This disorder is caused by mutation in the extracellular matrix protein 1 gene (ECM1). Clinical features include hoarseness and skin eruption due to widespread deposition of hyalin.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Hoarseness (1,139), Genetic Skin Diseases (3,548).
  4. Synonyms: Lipoproteinosis,  Urbach-Wiethe Disease


  

        

                    


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