354 top medical experts on Peutz-Jeghers Syndrome across 49 countries and 23 U.S. states, including 180 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Peutz-Jeghers Syndrome: A hereditary disease caused by autosomal dominant mutations involving chromosome 19. It is characterized by the presence of intestinal polyps, consistently in the jejunum, and mucocutaneous pigmentation with melanin spots of the lips, buccal mucosa, and digits.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Hereditary Neoplastic Syndromes (1,826), Intestinal Polyposis (1,345), Lentigo (931).
  4. Clinical Trials ClinicalTrials.gov : at least 13 including 4 Completed, 4 Recruiting
  5. Synonyms: Perioral Lentiginosis


  

        

                    


    Computing Expert Listing ...

);