210 top medical experts on LEOPARD Syndrome across 25 countries and 15 U.S. states, including 52 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. LEOPARD Syndrome: An autosomal dominant disorder with an acronym of its seven features (lentigo; electrocardiogram abnormalities; ocular hypertelorism; pulmonary stenosis; abnormal genitalia; retardation of growth; and deafness or sensorineural hearing loss). This syndrome is caused by mutations of ptpn11 gene encoding the non-receptor protein tyrosine phosphatase, type 11, and is an allelic to noonan syndrome. Features of leopard syndrome overlap with those of neurofibromatosis 1 which is caused by mutations in the neurofibromatosis 1 genes.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Craniofacial Abnormalities (2,386), Lentigo (931), Congenital Heart Defects (4,797), Multiple Abnormalities (3,208), Pulmonary Valve Stenosis (2,772).
  4. Clinical Trials ClinicalTrials.gov : at least 2 including 1 Completed, 1 Recruiting


  

        

                    


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