Results 81 to 90 of about 1,569,833 (157)

Sturge Weber Syndrome (Encephalotrigeminal Angiomatosis)

, 1984
Sturge Weber Syndrome (Encephalotrigeminal angiomatosis) with retinal evidence of central retinal vein occlusion. Anatomy: Retina. Pathology: Diffuse choroidal hemangioma; Glaucoma. Disease/Diagnosis: Sturge Weber Syndrome. Clinical: Port wine hemangioma
William F. Hoyt, MD
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Syndrome de Sturge-Weber : A propos d’un cas a Lome.

, 2015
Le syndrome de Sturge-Weber est une rare maladie congénitale, sporadique et non héréditaire. Il implique des malformations vasculaires de la peau (angiome cutané plan), des yeux et du cerveau (angiome leptoméningé). Les auteurs rapportent un cas révélé à 
Sonhaye, L, Balogou, E, Agoda-Koussema, LK, Adambounou, K, Adigo, AMY, Djagnikpo, O, N'Dakena, K, Adjenou, KV   +7 more
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Outcomes of Bilateral Sturge-Weber Syndrome [PDF]

, 2011
Researchers at Wayne State University School of Medicine, Detroit, MI studied 14 children with bilateral Sturge-Weber syndrome, representing 12.7% of a total of 110 patients with the ...
J Gordon Millichap
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Phakomatosis Pigmentovascularis Coexisting with a Variant of Sturge Weber Syndrome - A Rare Occurrence

Delhi Journal of Ophthalmology, 2019
The spectrum of phacomatoses is wide and they share common pathophysiological changes. The various entities widely studied and being reported are Sturge Weber Syndrome (SWS), Klippel Trenaunay Syndrome and Phakomatosis Pigmentovascularis (PPV).
Priyanka Singh, Nayana A. Potdar, Ankita Patil, Pritam K. Mohite, Chhaya A. Shinde, Pooja Bandivadekar   +5 more
doaj   +1 more source

A CASE OF STURGE-WEBER SYNDROME

Romanian Journal of Neurology, 2015
Encephalo-trigeminal angiomatosis of Sturge-Weber-Krabbe-Dimitri is a rare hereditary sporadic facomatosis, characterized by the presence of angiomatosis of brain lining vessels, face and eye capillaries. We present the case of a 25-year old girl with a birth mark, an facial angioma localized in the territory of the right ophthalmic nerve, also since ...
Daniela Trasca, Vlad Claudiu Stefanescu, Inimioara Mihaela Cojocaru   +2 more
openaire   +2 more sources

Surgical and Laser Treatment of Sturge-Weber Syndrome

, 2009
Sturge-Weber syndrome (also called encephalofacial or encephalotrigeminal angiomatosis) is a rare neurocutaneous syndrome characterized by facial port-wine stains in the trigeminal nerve distribution area.
CARELLA, SARA, SPINELLI, GRAZIANO, ONESTI, Maria Giuseppina, FIORAMONTI, Paolo, SCUDERI, Nicolo'   +4 more
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Intraoral capillary hemangioma in Sturge–Weber syndrome - A rare case report and its periodontal management

Journal of Indian Society of Periodontology
Sturge–Weber syndrome is often associated with different kinds of extraoral and intraoral manifestations, among which gingival overgrowth is one of the most common oral manifestations appreciated in the population. These oral manifestations can certainly
Sonia V Shinde, Neeta V Bhavsar
doaj   +1 more source

STURGE WEBER SYNDROME : A CASE REPORT [PDF]

, 2010
Sturge-Weber syndrome is a rare nonhereditary developmental condition that is characterized by a hamartomatous vascular proliferation involving the tissue of brain and face. The clinical features are characterized by port wine nevus following one or more
김성오, 이제호, 최형준, 최병재   +3 more
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Sturge Weber Syndrome (Encephalotrigeminal Angiomatosis)

, 1963
Sturge Weber Syndrome (Encephalotrigeminal angiomatosis); Color of the retina is deep red (sometimes called tomato catsup) due to a four fold thickening of the choroidal vascular bed. Glaucomatous cupping of the optic nerve.
William F. Hoyt, MD
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Hypomelanosis of Ito and Sturge-Weber Syndrome Without Facial Nevus: An Association or a New Syndrome?

, 2009
Sturge-Weber syndrome without facial nevus is rare. Twenty-four cases were previously reported. Although hypomelanosis of Ito is a relatively common disorder, there was only one previous case in association with Sturge-Weber syndrome.
AYSÜN, SABİHA, Kantar, Asli, Degerliyurt, Aydan, Ceylaner, Serdar   +3 more
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