354 top medical experts on Dyskeratosis Congenita across 38 countries and 20 U.S. states, including 205 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Dyskeratosis Congenita: A predominantly X-linked recessive syndrome characterized by a triad of reticular skin pigmentation, nail dystrophy and leukoplakia of mucous membranes. Oral and dental abnormalities may also be present. Complications are a predisposition to malignancy and bone marrow involvement with pancytopenia. (from Int J Paediatr Dent 2000 Dec;10(4):328-34) The X-linked form is also known as Zinsser-Cole-Engman syndrome and involves the gene which encodes a highly conserved protein called dyskerin.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): X-Linked Genetic Diseases (2,304), Genetic Skin Diseases (3,548), Congenital Bone Marrow Failure Syndromes (644), Skin Abnormalities (2,933).
  4. Clinical Trials ClinicalTrials.gov : at least 13 including 4 Completed, 7 Recruiting
  5. Synonyms: X-Linked Dyskeratosis Congenita,  Zinsser-Cole-Engman Syndrome


  

        

                    


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