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.
Year introduced: 1991(1975)
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Subheadings:
Tree Number(s): C04.557.645.375.850, C10.562.800, C14.907.077.850
MeSH Unique ID: D013341
Entry Terms:
- Sturge Weber Syndrome
- Syndrome, Sturge-Weber
- 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
- Sturge-Weber-Krabbe Syndrome
- Sturge Weber Krabbe Syndrome
- Syndrome, Sturge-Weber-Krabbe
- Angiomatosis Oculoorbital-Thalamic Syndrome
- Encephalofacial Hemangiomatosis Syndrome
- Hemangiomatosis Syndrome, Encephalofacial
- Syndrome, Encephalofacial Hemangiomatosis
- Meningo-Oculo-Facial Angiomatosis
- Angiomatosis, Meningo-Oculo-Facial
- Meningo Oculo Facial Angiomatosis
- Meningofacial Angiomatosis-Cerebral Calcification Syndrome
- Neuroretinoangiomatosis
- Parkes Weber Syndrome
- Syndrome, Parkes Weber
- Parkes-Weber Syndrome
- Syndrome, Parkes-Weber