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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.
6 lip 2024 · The phakomatoses (also known as neurocutaneous syndromes) are a heterogeneous group of disorders most characterized by the involvement of structures that arise from the embryonic ectoderm (thus central nervous system, skin, and eyes), although other systems may also be involved.
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 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.
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 neurocutaneous disorder characterized by angiomatosis of the skin, eye, and meninges. The expression of the syndrome is variable 1 but typically manifests as facial port-wine stain (PWS), ocular choroidal hemangiomas, and cerebral pial angiomatosis.
Sturge-Weber Syndrome. Background: Rare, congenital, sporadic, neurocutaneous, and vascular disorder caused by somatic mutations in fetal ectodermal tissues that cause dysregulation of capillary blood vessel formation.
