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18 sie 2024 · Sturge-Weber syndrome, also known as encephalotrigeminal angiomatosis or encephalofacial angiomatosis, is a phakomatosis characterized by facial port-wine nevus (capillary malformation) and pial angiomas. It is part of a wide spectrum of possible phenotypes included in the cerebrofacial arteriovenous metameric syndrome (CAMS).
10 lis 2014 · Sturge-Weber syndrome (SWS) is a rare neurocutaneous syndrome, usually sporadic in nature, which is a result of occlusion/stasis of the persistent fetal vasculature resulting in cortical anoxia. 1 It is characterised by facial port-wine stain, leptomeningeal angiomatosis, congenital glaucoma, intractable epilepsy and progressive mental ...
Sturge-Weber syndrome (SWS) is a rare neurocutaneous syndrome, usually sporadic in nature, which is a result of occlusion/stasis of the persistent fetal vasculature resulting in cortical anoxia.1 It is characterised by facial port-wine stain, leptomeningeal angiomatosis, congenital glaucoma, intractable epilepsy and progressive mental ...
Sturge-Weber syndrome is one of the neurocutaneous syndromes and was first described by Sturge in 1879 [1]. Weber demonstrated the characteristic intracranial calcifications in 1929 [2].
Sturge-Weber syndrome is a neurocutaneous syndrome that includes facial and leptomeningeal angiomas. Imaging findings include cerebral lobar atrophy, brain calcifications, choroid plexus enlargement, cranial diploë prominence, and venous abnormalities.
Gautam M, Sturge-Weber syndrome. Case study, Radiopaedia.org (Accessed on 29 Jun 2024) https://doi.org/10.53347/rID-92019
14 lip 2024 · Sturge-Weber Syndrome (SWS), also known as encephalotrigeminal angiomatosis, is a neurocutaneous disorder with vascular skin lesions (port-wine stains), leptomeningeal angiomatosis, and ocular abnormalities, typically in the form of glaucoma.
