Sturge Weber Syndrome (SWS) is a random, non-hereditary congenital illness with an unknown cause. It manifests itself in a wide range of ways, including cutaneous, neurologic, ophthalmic, and oral symptoms (1). It happens as a result of the embryonic vascular plexus persisting abnormally (2). Topical cutaneous angiomas known as "Port-wine stains" o
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