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Complete Tri Symptomatic Sturge Weber Syndrome - A case report with review of literature

Journal of Indian Academy of Oral Medicine and Radiology, 2007
Sturge-Weber syndrome (SWS) belongs to a group of disorders collectively known as the phakomatoses ("mother-spot" diseases). It consists of congenital hamartomatous malformations that may affect the eye, skin, and central nervous system at different ...
Karthik Hegde, R Gopakumar, Subhas Babu, S Giridhar Naidu, Vidya Ajila, R Kamala   +5 more
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A Case of Congenital Glaucoma in a 5-Year-Old Patient With Sturge–Weber Syndrome and Oculodermal Melanocytosis

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   +1 more source

Walsh & Hoyt: Sturge-Weber Syndrome Encephalotrigeminal Angiomatosis

, 2005
In 1879, Sturge described a combination of ipsilateral facial hemangioma and buphthalmos in a child with contralateral seizures. He suspected that the facial angioma was associated with an intracranial hemangioma, which was confirmed at autopsy.
John Kerrison, MD
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Síndrome de Sturge-Weber

, 2009
Ocho imágenes de un cerebro afectado por el síndrome de Sturge-Weber.Eight pictures of a brain affected by the Sturge-Weber ...
Iglesias Rozas, José Rafael, 1942-
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Sturge -Weber Syndrome - Three Classic variants

Journal of Indian Academy of Oral Medicine and Radiology, 2006
Sturge-Weber syndrome (SWS), also known as encephalotrigeminal angiomatosis, a sporadic, non-familial, congenital disorder consists of congenital hamartomatous malformations that may affect the eye, skin and central nervous system at different times ...
R S Sathawane, R N Mody, Apeksha Balpande   +2 more
doaj  

Differentiating the effects of epilepsy in children with Sturge-Weber syndrome

, 2006
Sturge-Weber Syndrome is a rare neurocutaneous disorder associated with glaucoma, port-wine stain birthmarks, and abnormal vasculature of the brain that often results in epilepsy. Behavioral and academic sequelae have also been reported.
Raches, Darcy
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Sturge-Weber syndrome

, 2010
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Sturge-Weber syndrome and glaucoma

Optometry - Journal of the American Optometric Association, 2011
Sturge-Weber syndrome (SWS) belongs to a group of disorders known as the phakomatoses. It is characterized by congenital hamartomatous malformations involving the eye, skin, and central nervous system. Several ocular complications are associated with SWS, including glaucoma.A 66-year-old black man presented with a history of SWS and previously ...
Joseph Sówka
exaly   +3 more sources

Sturge-Weber Syndrome

Advances in Neonatal Care, 2014
Sturge-Weber syndrome (SWS) is a rare, congenital neurocutaneous condition (affecting both the skin and the brain) characterized by a facial port-wine stain located specifically on the ophthalmic branch of the trigeminal nerve, cerebral vascular abnormalities, and potential eye involvement.
Sarah J, Garro, Wanda T, Bradshaw
openaire   +3 more sources

Headache in Sturge-Weber Syndrome

Headache, 1994
SYNOPSIS Based on reports of headache in arteriovenous malformations and epilepsy, one would predict that the prevalence of migraine headache in the Sturge‐Weber syndrome would be higher than in the general population. A questionnaire designed to determine the prevalence and type of headache by IHS criteria was sent ...
exaly   +3 more sources