Adroos, NaroshaSmal, JanetSuleman, Farhana Ebrahim2015-12-082015-12-082015-08-14Adroos N, Smal J, Suleman FE. Double trouble: Bilateral cerebral involvement in Sturge-Weber syndrome. S Afr J Rad. 2015;19(1); Art. #760, 4 pages. http://dx.DOI.org/ 10.4102/sajr.v19i1.760.1027-202X (print)2078-6778 (online)10.4102/sajr.v19i1.760http://hdl.handle.net/2263/51111Sturge-Weber syndrome, also known as encephalotrigeminal angiomatosis or meningofacial angiomatosis, is characterised in its classical form by a congenital, usually unilateral, ‘portwine stain’ (capillary naevus) on the face, convulsions, typical intracranial calcification and some degree of mental retardation and hemiparesis. The clinical correlation of intractable seizures with the presence of bilateral intracranial disease has management and prognostic implications, thus making the presence of bilateral disease an important factor to all those involved in the management of the child with Sturge-Weber syndrome.en© 2015. The Authors. Licensee: AOSIS OpenJournals. This work is licensed under the Creative Commons Attribution License.Sturge-Weber syndromeEncephalotrigeminal angiomatosisMeningofacial angiomatosisPortwine stain (capillary naevus)Bilateral intracranial diseaseConvulsionsIntracranial calcificationMental retardationHemiparesisArticle