280 top medical experts on Cockayne Syndrome across 36 countries and 18 U.S. states, including 74 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Cockayne Syndrome: A syndrome characterized by multiple system abnormalities including dwarfism; photosensitivity disorders; premature aging; and hearing loss. It is caused by mutations of a number of autosomal recessive genes encoding proteins that involve transcriptional-coupled DNA repair processes. Cockayne syndrome is classified by the severity and age of onset. Type I (classical; CSA) is early childhood onset in the second year of life; type II (congenital; CSB) is early onset at birth with severe symptoms; type III (xeroderma pigmentosum; XP) is late childhood onset with mild symptoms.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Multiple Abnormalities (3,208), Dwarfism (1,222), Nervous System Heredodegenerative Disorders (865), DNA Repair-Deficiency Disorders (751).
  4. Clinical Trials ClinicalTrials.gov : at least 9 including 2 Completed, 5 Recruiting
  5. Synonyms: Progeria-Like Syndrome


  

        

                    


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