192 top medical experts on Prolidase Deficiency across 15 countries and 6 U.S. states, including 22 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Prolidase Deficiency: Rare autosomal recessive disorder of metabolism due to mutations in the prolidase gene. It is characterized by recurrent lower extremity skin ulcers, recurrent infections, and facies, often with intellectual disability.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Genetic Skin Diseases (3,548), Inborn Errors Amino Acid Metabolism (1,295), Multiple Abnormalities (3,208), Skin Abnormalities (2,933).
  4. Clinical Trials ClinicalTrials.gov : at least 1 including 1 Completed


  

        

                    


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