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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.
20 paź 2022 · Study by Dymerska et al 24 suggests that size of facial PWB correlates with neurological severity ratings for patients ages 6 and above with SWS brain involvement. The size and location of PWB in combination with brain MRI images can be helpful in predicting the severity of neurological dysfunction.
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 ...
1 maj 2023 · Diagnosis of Sturge-Weber syndrome is based on typical clinical symptoms, facial appearance, and brain magnetic resonance imaging (MRI) findings. An ophthalmic examination is required to rule out glaucoma.
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 brain involvement is marked by a leptomeningeal vascular malformation on contrast enhanced MRI images (Figure322A Dilated and 2B). deep draining vessels underlying the affected cortical region and enhancement of the choroid plexus on the involved side are also often present in older children and adults.
Question What are clinical practice guidelines for treatment and management of port-wine birthmarks, including those associated with Sturge-Weber syndrome? Findings In this consensus statement, 10 key recommendations for treatment of port-wine birthmarks were formulated.