328 top medical experts on Sturge-Weber Syndrome across 43 countries and 28 U.S. states, including 218 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Sturge-Weber Syndrome: A non-inherited congenital condition with vascular and neurological abnormalities. It is characterized by facial vascular nevi (port-wine stain), and capillary angiomatosis of intracranial membranes (meninges; choroid). Neurological features include epilepsy; cognitive deficits; glaucoma; and visual defects.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Hemangioma (2,319), Angiomatosis (1,165), Neurocutaneous Syndromes (1,959).
  4. Clinical Trials ClinicalTrials.gov : at least 17 including 2 Active, 8 Completed, 4 Recruiting
  5. Synonyms: Neuroretinoangiomatosis,  Sturge-Weber Phakomatosis


  

        

                    


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