209 top medical experts on Rothmund-Thomson Syndrome across 24 countries and 7 U.S. states, including 41 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Rothmund-Thomson Syndrome: An autosomal recessive syndrome occurring principally in females, characterized by the presence of reticulated, atrophic, hyperpigmented, telangiectatic cutaneous plaques, often accompanied by juvenile cataracts, saddle nose, congenital bone defects, disturbances in the growth of hair; nails; and teeth; and hypogonadism.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Diseases Newborn Infant (2,780), DNA Repair-Deficiency Disorders (751), Genetic Skin Diseases (3,548), Skin Abnormalities (2,933).
  4. Clinical Trials ClinicalTrials.gov : at least 2 including 1 Completed, 1 Recruiting
  5. Synonyms: Poikiloderma Congenitale


  

        

                    


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