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Sturge-Weber Syndrome [PDF]

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, Prasanth Balasubramanium, Ram Nampoothiri, Ashish Bhalla, Subhash Varma   +4 more
doaj   +5 more sources

Sturge–Weber syndrome

QJM - Monthly Journal of the Association of Physicians
Daniel Xin Zhang
exaly   +4 more sources

Sturge-Weber syndrome

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, Subramanium Gokulanathan, Ramakrishnan Swamy Ahathya, Gubernath, Rajkumar Daniel, Shanmugasundaram   +5 more
doaj   +3 more sources

Clinical Validation of a Fast MRI Method to Evaluate Brain Vascular and Parenchymal Abnormalities in Sturge-Weber Syndrome. [PDF]

J Magn Reson Imaging
ABSTRACT Background Sturge‐Weber syndrome (SWS) is a rare neurocutaneous disorder associated with venous capillary malformations, atrophy, and calcifications. Longitudinal imaging is limited by risks of sedation and gadolinium exposure in children.
McKay SG, Chen Y, Haacke EM, Xuan Y, Luat AF, Juhász C.   +5 more
europepmc   +2 more sources

Sturge Weber Syndrome

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, S.M. Abu Ahsan, Md. Shafiqul lslam   +2 more
doaj   +6 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, Paneerselvam Venkatachalam   +1 more
doaj   +3 more sources

A Case of Congenital Glaucoma in a 5-Year-Old Patient With Sturge–Weber Syndrome and Oculodermal Melanocytosis [PDF]

Case Reports in Ophthalmological Medicine
Conclusions: It is possible to achieve intraocular pressure control in a patient with congenital glaucoma associated with Sturge–Weber syndrome and oculodermal melanocytosis using staged Ahmed tube insertion.
Param Shukla, Miriam Habiel
doaj   +2 more sources

Sturge-Weber Syndrome [PDF]

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

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, Bishal Kunwor, Suchit Thapa Chhetri, Sanath Nepal, Khusbu Sedhai   +4 more
doaj   +1 more source

Progressive retinal vessel malformation in a premature infant with Sturge-Weber syndrome: a case report and a literature review of ocular manifestations in Sturge-Weber syndrome

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, Jian Cao, Eun Young Choi, Yun Li   +3 more
doaj   +1 more source