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Sturge-Weber Syndrome: A Case Report [PDF]
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
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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 +5 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 Bachur, Anne M. Comi
+7 more sources
QJM: An International Journal of Medicine, 2018 Sturge-Weber syndrome (SWS) is characterized by the association of capillary malformation of the face (CM), leptomeningeal angiomatosis, and glaucoma (Fig. 35.1). SWS is classified into three types (Table 35.1) (Roach, Pediatr Clin N Am 39(4):591–620, 1992).
Tsung‐Han Ho +4 more
+7 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
Sturge–Weber Syndrome with Bilateral Port-Wine Stain [PDF]
Case Reports in Pediatrics, 2022 Sturge–Weber syndrome is a rare congenital neurocutaneous disorder characterized by dermatological, ophthalmological, and neurological manifestations. It occurs due to abnormal persistence of embryonic vascular plexus.
Bishnu Deep Pathak +5 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 +7 more sources
Phakomatosis pigmentovascularis presenting with Sturge-Weber syndrome and Klippel-Trenaunay syndrome
Indian Journal of Dermatology, 2015 Phakomatosis pigmentovascularis (PPV) is a rare cutaneous disorder characterized by combination of capillary malformation and other pigmented naevi. Four types and two subtypes have been described where subtype ′a′ present only with cutaneous form and ...
Sumit Sen +4 more
doaj +2 more sources
No shinkei geka. Neurological surgery, 2010 Sturge-Weber syndrome (SWS) is a rare neurocutaneous syndrome characterized by intracranial leptomeningeal angioma, facial port-wine nevi, and glaucoma. Diagnosis is relatively easy because of the facial angioma and MRI findings, but evaluating severity is difficult.
Ammar Haouimi
+5 more sources
Double trouble: Bilateral cerebral involvement in Sturge-Weber syndrome
South African Journal of Radiology, 2015 Sturge-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 ...
Narosha Adroos +2 more
doaj +3 more sources