RT - Journal TY - JOUR A1 - Verma, Kalpana A1 - Thakur, Seema A1 - Justa, Ashish T1 - Sturge–Weber syndrome YR - 2021/7/1 JF - Indian Journal of Oral Health and Research JO - Indian J Oral Health Res SP - 74 OP - 77 VO - 7 IS - 2 UL - https://www.ijohr.org/article.asp?issn=2393-8692;year=2021;volume=7;issue=2;spage=74;epage=77;aulast=Verma;t=5 DO - 10.4103/ijohr.ijohr_25_20 N2 - The Sturge–Weber syndrome (SWS) or encephalotrigeminal angiomatosis is specifically congenital, nonhereditary, and rare condition of unknown etiology. It belongs to a group of disorders collectively known as the phakomatoses (“motherspot” diseases). In its complete tri-symptomatic form, SWS is physically characterized by port-wine stains over the trigeminal area, leptomeningeal angiomas usually over the parieto-occipital region, and eye abnormalities. Clinical manifestation of SWS depends on the affected organs and can include seizures, mental retardation, and glaucoma. ER -