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.

Descriptor ID	D013341
MeSH Number(s)	C04.557.645.375.850 C10.562.800 C14.907.077.850
Concept/Terms	Sturge-Weber Syndrome Sturge-Weber Syndrome Sturge Weber Syndrome Syndrome, Sturge-Weber Encephalofacial Hemangiomatosis Syndrome Encephalofacial Hemangiomatosis Syndromes Hemangiomatosis Syndrome, Encephalofacial Hemangiomatosis Syndromes, Encephalofacial Syndrome, Encephalofacial Hemangiomatosis Syndromes, Encephalofacial Hemangiomatosis Meningo-Oculo-Facial Angiomatosis Angiomatoses, Meningo-Oculo-Facial Angiomatosis, Meningo-Oculo-Facial Meningo Oculo Facial Angiomatosis Meningo-Oculo-Facial Angiomatoses Meningofacial Angiomatosis-Cerebral Calcification Syndrome Meningofacial Angiomatosis Cerebral Calcification Syndrome Neuroretinoangiomatosis Neuroretinoangiomatoses Sturge-Weber-Krabbe Syndrome Sturge Weber Krabbe Syndrome Syndrome, Sturge-Weber-Krabbe Phakomatosis, Sturge-Weber Phakomatosis, Sturge Weber Sturge-Weber Phakomatosis Sturge Disease Sturge Syndrome Syndrome, Sturge Sturge's Syndrome Syndrome, Sturge's Sturge-Kalischer-Weber Syndrome Sturge Kalischer Weber Syndrome Syndrome, Sturge-Kalischer-Weber Sturge-Weber-Dimitri Syndrome Sturge Weber Dimitri Syndrome Syndrome, Sturge-Weber-Dimitri Angiomatosis Oculoorbital-Thalamic Syndrome Parkes Weber Syndrome Parkes Weber Syndromes Syndrome, Parkes Weber Syndromes, Parkes Weber Weber Syndrome, Parkes Weber Syndromes, Parkes

Below are MeSH descriptors whose meaning is more general than "Sturge-Weber Syndrome".

Below are MeSH descriptors whose meaning is related to "Sturge-Weber Syndrome".

Below are MeSH descriptors whose meaning is more specific than "Sturge-Weber Syndrome".