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.
Also Known As:
Sturge-Kalischer-Weber Syndrome; Sturge-Weber-Dimitri Syndrome; Angiomatosis Oculoorbital-Thalamic Syndrome; Encephalofacial Hemangiomatosis Syndrome; Meningo-Oculo-Facial Angiomatosis; Meningofacial Angiomatosis-Cerebral Calcification Syndrome; Parkes Weber Syndrome; Parkes-Weber Syndrome; Sturge Disease; Sturge Syndrome; Sturge's Syndrome; Sturge-Weber-Krabbe Syndrome; Angiomatosis, Meningo-Oculo-Facial; Hemangiomatosis Syndrome, Encephalofacial; Meningo Oculo Facial Angiomatosis; Phakomatosis, Sturge Weber; Sturge Kalischer Weber Syndrome; Sturge Weber Dimitri Syndrome; Sturge Weber Krabbe Syndrome; Sturge Weber Syndrome; Sturge-Weber Phakomatosis; Syndrome, Encephalofacial Hemangiomatosis; Syndrome, Parkes Weber; Syndrome, Parkes-Weber; Syndrome, Sturge; Syndrome, Sturge's; Syndrome, Sturge-Kalischer-Weber; Syndrome, Sturge-Weber; Syndrome, Sturge-Weber-Dimitri; Syndrome, Sturge-Weber-Krabbe; Neuroretinoangiomatosis; Phakomatosis, Sturge-Weber