Results 11 to 20 of about 3,465 (171)
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
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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
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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
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Diagnostic Challenge of Sturge Weber Syndrome Phenotype in Camp Setting
NMO Journal, 2022 Sturge Weber angiomatosis is a non-developmental, rare condition with a vascular hamartomata's involving the tissues of brain and face. We report herewith a case presenting with recurrent seizures and facial port wine stain in a camp of tribal area in ...
Annvi singh +2 more
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Periodontal management of gingival enlargement associated with Sturge-Weber syndrome
Journal of Indian Society of Periodontology, 2013 The Sturge-Weber syndrome is a rare uncommon neurocutaneous disorders with angiomas involving the leptomeninges (Leptomeningeal Angiomas) and skin of the face, typically in the ophthalmic (V1) and maxillary (V2) distributions of the trigeminal nerve. The
Sugumari Elavarasu +2 more
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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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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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Severe, Infantile-Onset Seizure Pattern in Sturge-Weber Syndrome
Pediatric Neurology Briefs, 2009 Researchers at the Hunter Nelson Sturge-Weber Center, Kennedy Krieger Institute, Baltimore, reviewed the records of 100 consecutive children and adults with confirmed Sturge-Weber syndrome (SWS) to determine the nature and prognosis of associated ...
J Gordon Millichap
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Sturge-Weber Syndrome with Osteohypertrophy of Maxilla
Case Reports in Pediatrics, 2013 Sturge-Weber syndrome is a rare nonhereditary developmental condition with neurological and skin disorder, characterized by presence of port wine stain on the face along with ocular disorders, oral manifestations and leptomeningeal angiomas.
Prashant Babaji +7 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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