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.
- 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.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Broader Categories (#Experts): Hemangioma (2,319), Angiomatosis (1,165), Neurocutaneous Syndromes (1,959).
- Clinical Trials : at least 17 including 2 Active, 8 Completed, 4 Recruiting
- Synonyms: Neuroretinoangiomatosis, Sturge-Weber Phakomatosis
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