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Sturge-Weber Syndrome: A Case Report
Journal of Nepal Medical Association, 2023 Sturge-Weber syndrome is a rare congenital neurocutaneous syndrome with an incidence of 1 in 50000 characterised by facial capillary malformation and vascular anomalies in the brain and eye.
Sunil Timilsina +4 more
doaj +2 more sources
Bangabandhu Sheikh Mujib Medical University Journal, 2016 Sturge weber syndrome is a rare sporadic condition of mesodermal phacomatosis, also called encephalotrigeminal angiomatosis (synonyms : fourth phacomatosis or mother spot), is a neurocutaneous disorder with angiomas that involve the leptomeninges ...
Kazi Nilufar Moly +2 more
doaj +6 more sources
Journal of Clinical and Diagnostic Research, 2017 A 6-year-old girl was brought to the emergency department with sudden onset of weakness in the left arm and leg. Physical examination and MRI suggested a diagnosis of the Sturge–Weber syndrome.
Bharath A Chhabria +4 more
doaj +5 more sources
Journal of Pharmacy and Bioallied Sciences, 2012 Encephalotrigeminal angiomatosis (Sturge-Weber syndrome) is a rather uncommon congenital condition characterized by the combination of venous angioma of the leptomeninges over the cerebral cortex with ipsilateral angiomatous lesions of the face, and ...
Natarajan Manivannan +5 more
doaj +4 more sources
Sturge–Weber syndrome and glaucoma
Journal of Pharmacy and Bioallied Sciences, 2021 Sturge–Weber syndrome (SWS) is a neurocutaneous syndrome characterized by capillary venous malformations in the skin, eye, and brain with the occurrence of angiomas of the face, choroid, and leptomeninges.
Sambavi Anbuselvan +1 more
doaj +3 more sources
Current Treatment Options in Neurology, 2013 We try to see the babies prior to the onset of symptoms so that their parents can receive anticipatory guidance regarding seizures and how to recognize and respond to them and so that proper referrals to ophthalmology can be made. If there is any concern on history, exam, or EEG then we obtain a magnetic resonance imaging (MRI) with contrast.
Catherine D, Bachur, Anne M, Comi
+6 more sources
BMC Ophthalmology, 2021 Background Sturge-Weber syndrome is a disorder marked by a distinctive facial capillary malformation, neurological abnormalities, and ocular abnormalities such as glaucoma and choroidal hemangioma.
Zhengping Hu +3 more
doaj +1 more source
Annals of Dermatology, 2011 Sturge-Weber syndrome (SWS) is a neurocutaneous syndrome, characterized by the association of facial port-wine hemangiomas in the trigeminal nerve distribution area, with vascular malformation(s) of the brain (leptomeningeal angioma) with or without glaucoma.
Chen, Ling +4 more
openaire +4 more sources
Birthmark: Journey from aesthetic to unalluring
Journal of Indian Academy of Oral Medicine and Radiology, 2020 Encephalotrigeminal Angiomatosis, also known as Sturge Weber Syndrome (SWS), Dimitri disease, Sturge Kalischer Weber Syndrome is specifically non familial, congenital rare disorder consisting of hamartomatous malformations that may affect eye, skin, and ...
Sakshi Sharma +3 more
doaj +1 more source
Sturge Weber syndrome, when brain CT is enough for diagnosis: about a case
The Pan African Medical Journal, 2020 One of the main manifestations of Sturge Weber syndrome is seizures. We report the case of a child received in the context of generalized seizures and in whom a cerebral contrast CT was sufficient to make the diagnosis of Sturge Weber syndrome.
Ibrahima Niang +6 more
doaj +1 more source