237 top medical experts on Costello Syndrome across 21 countries and 24 U.S. states, including 79 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Costello Syndrome: Rare congenital disorder with multiple anomalies including: characteristic dysmorphic craniofacial features, musculoskeletal abnormalities, neurocognitive delay, and high prevalence of cancer. Germline mutations in H-Ras protein can cause Costello syndrome. Costello syndrome shows early phenotypic overlap with other disorders that involve MAP kinase signaling system (e.g., noonan syndrome and cardiofaciocutaneous syndrome).
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Inborn Genetic Diseases (2,477), Craniofacial Abnormalities (2,386), Multiple Abnormalities (3,208).
  4. Clinical Trials ClinicalTrials.gov : at least 4 including 1 Completed, 2 Recruiting
  5. Synonyms: Faciocutaneoskeletal Syndrome


  

        

                    


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