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Bilateral Sturge-Weber Syndrome and glaucoma controlled with Ahmed valve implant
Revista Brasileira de Oftalmologia, 2015 Sturge-Weber Syndrome is a rare neuro-oculocutaneous disorder. The authors describe the case of a 13 years old boy, presented with bilateral Sturge-Weber Syndrome and glaucoma. Surgical treatment with Ahmed valve implantation in both eyes was carried out
Marcelo Jarczun Kac +3 more
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Sturge-Weber Syndrome Type III [PDF]
, 2018 Sturge-Weber syndrome (SWS) is a neurogenetic disease with an incidence of 1 in 20.000-50.000 live births. The less common form, which can be difficult to diagnose and only involves leptomeningeal angioma, has been defined as Type III SWS.
Tekgul, Hasan +10 more
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Annals of Indian Academy of Neurology, 2014 The Sturge Weber syndrome is characterized by developmental delay, seizures in infancy, unilateral cutaneous lesions with ipsilateral leptomeningeal enhancement. We report an unusual presentation of Sturge Weber syndrome with bilateral port wine nevus on
Kundan Mittal +4 more
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Epilepsy in Sturge-Weber syndrome: a literature review and description of a clinical case
Эпилепсия и пароксизмальные состояния, 2020 The Struge-Weber syndrome is the third most common neurodermal disease after neurofibromatosis and tuberous sclerosis. This disease is not inherited, but occurs exclusively sporadically, both in men and in women, and in all races and ethnic groups. In 90%
N. I. Shova +3 more
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Surgical treatment of the patient with Sturge-Weber syndrome - a case report
Journal of Education, Health and Sport, 2017 Vascular malformations associated with genetic syndromes lead to dysfunction of human body organs by blood supply impairment. Disorders in the structure of blood vessels walls result in developing pathological lesions called hemangiomas.
Adrian Gnatek +2 more
doaj +3 more sources
Sturge-Weber syndrome without facial nevus [PDF]
, 2013 Sturge-Weber syndrome is a rare neurocutaneous disorder. Coexistence of facial nevus with epilepsy often suggests the diagnosis of Sturge-Weber syndrome. However, the diagnosis becomes more difficult when there is no facial nevus. Radiologic examinations
Guler, Ibrahim +2 more
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Nepal Journal of Neuroscience, 2019 Sturge-weber syndrome is a type of neurocutaneous syndrome/ neurooculo cutaneous/ phakomatoses that is characterized by facial capillary Port Wine stain, leptomeningealangioma and glaucoma with a incidence of 1 per 20-50,000 live births.
Yam Bahadur Roka
doaj +1 more source
Epilepsia Open, EarlyView.Abstract Objective Epilepsy affects approximately 50 million people worldwide and, although primarily attributed to neuronal dysfunction, increasing evidence highlights a critical role of glial cells, particularly astrocytes, in the pathophysiological mechanisms.
Chiara Lötzsch +5 more
wiley +1 more source
Sturge-Weber syndrome with ocular involvement [PDF]
Revista Brasileira de OftalmologiaSturge-Weber syndrome is a rare sporadic and congenital neurocutaneous disease characterized primarily by the presence of cutaneous and extracutaneous capillary malformations.
Oueslati Yassin +5 more
doaj +1 more source
Infantile Sturge-Weber Syndrome with Hypointense White Matter on T2-weighted MR images [PDF]
, 1996 The implication of hypointense white matter on T2- weighted MR images in infants with Sturge-Weber syndrome is a subject of recent controversy. We report a case of infantile Sturge-Weber syndrome with decreased white matter signal on T2-weighted MR ...
Morikawa, Minoru +5 more
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