Sturge-Weber Syndrome

**Definition:** 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.

**Tree numbers:** - C04.557.645.375.850 - C10.562.800 - C14.907.077.850

**Synonyms:** - Phakomatosis, Sturge-Weber - Sturge Disease - Sturge Syndrome - Sturge's Syndrome - Sturge-Kalischer-Weber Syndrome - Sturge-Weber-Dimitri Syndrome - Sturge-Weber-Krabbe Syndrome - Angiomatosis Oculoorbital-Thalamic Syndrome - Encephalofacial Hemangiomatosis Syndrome - Meningo-Oculo-Facial Angiomatosis - Meningofacial Angiomatosis-Cerebral Calcification Syndrome - Neuroretinoangiomatosis