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Sturge–Weber syndrome: an update for the pediatrician
World Journal of PediatricsSturge-Weber syndrome (SWS) is a rare congenital neurocutaneous disorder characterized by the simultaneous presence of both cutaneous and extracutaneous capillary malformations. SWS usually presents as a facial port-wine birthmark, with a varying presence of leptomeningeal capillary malformations and ocular vascular abnormalities.
Emilie Dingenen +3 more
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Advances in Sturge-Weber syndrome
Current Opinion in Neurology, 2006Recent neuroimaging, clinical and molecular neuropathologic studies have provided new insights into the neurologic aspects of Sturge-Weber syndrome and are summarized here.Molecular studies suggest that abnormal brain blood vessel vasoactive and extracellular matrix molecule expression, as well as aberrant brain vascular innervation, contribute to the ...
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Characteristics, surgical outcomes, and influential factors of epilepsy in Sturge-Weber syndrome.
Brain, 2022Meng Zhao, Yongxing Sun, Yuguang Guan
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Aspirin Use in Sturge-Weber Syndrome: Side Effects and Clinical Outcomes
Journal of Child Neurology, 2013T Andrew Zabel, Eboni I Lance, Anne Comi
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