Results 11 to 20 of about 1,569,833 (157)

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, S Thanga Kumaran, P K Sasi Kumar   +2 more
doaj   +2 more sources

Secondary Glaucoma in Sturge–Weber Syndrome

Okulistyka
Sturge–Weber syndrome is a congenital neurocutaneous disorder involving abnormalities of blood vessels (hemangiomas) in the brain, face, and eyes. It is not hereditary or genetic, but it is present from birth.
Bożena Romanowska-Dixon, Joanna Kobylarz, Magdalena Dębicka-Kumela, Joanna Kowal, Agnieszka Nowak, Natalia Mackiewicz, Izabella Karska-Basta   +6 more
doaj   +2 more sources

Sturge-Weber Syndrome with Osteohypertrophy of Maxilla [PDF]

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, Anju Bansal, Gopal Krishna Choudhury, Rashmita Nayak, Ashok Kodangala Prabhakar, Nagarathna Suratkal, Veena Raju, Suresh S. Kamble   +7 more
doaj   +2 more sources

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
doaj   +2 more sources

Overlap of Sturge-Weber syndrome and Klippel-Trenaunay syndrome

Indian Journal of Dermatology, 2011
Sturge-Weber syndrome is a rare sporadic condition of mesodermal phakomatosis, characterized by purple-colored flat cutaneous cranial (face) hemangiomas (most commonly along the trigeminal nerve), glaucoma and vascular lesions in the ipsilateral brain ...
Radheshyam Purkait, Tryambak Samanta, Tapankumar Sinhamahapatra, Mridula Chatterjee   +3 more
doaj   +2 more sources

Double trouble: Bilateral cerebral involvement in Sturge-Weber syndrome [PDF]

South African Journal of Radiology, 2015
Sturge-Weber syndrome, also known as encephalotrigeminal angiomatosis or meningofacial angiomatosis, is characterised in its classical form by a congenital, usually unilateral, ‘portwine stain’ (capillary naevus) on the face, convulsions, typical ...
Narosha Adroos, Janet Smal, Farhana E. Suleman   +2 more
doaj   +2 more sources

Phakomatosis pigmentovascularis presenting with Sturge-Weber syndrome and Klippel-Trenaunay syndrome

Indian Journal of Dermatology, 2015
Phakomatosis pigmentovascularis (PPV) is a rare cutaneous disorder characterized by combination of capillary malformation and other pigmented naevi. Four types and two subtypes have been described where subtype ′a′ present only with cutaneous form and ...
Sumit Sen, Sanchaita Bala, Chinmay Halder, Rahul Ahar, Anusree Gangopadhyay   +4 more
doaj   +2 more sources

Undiagnosed Epileptic Case Since Childhood of Sturge-Weber Syndrome: First Case Report from Somalia [PDF]

International Medical Case Reports Journal
Said Abdi Mohamed,1 Nor Osman Sidow,1,2 Bakar Ali Adam,1 Mohamed Sheikh Hassan,1,3 Abdiwahid Ahmed Ibrahim,1 Mohamed Farah Osman,1 Abdulkadir Ahmed,1 Abdullahi Ali Roble4 1Department of Neurology, Mogadishu-Somalia Turkey Recep Tayyip Erdoğan ...
Mohamed SA, Sidow NO, Adam BA, Hassan MS, Ibrahim AA, Osman MF, Ahmed A, Roble AA   +7 more
doaj   +1 more source

Predicting and Preventing Epilepsy in Sturge-Weber Syndrome? [PDF]

Pediatric Neurology Briefs, 2016
Investigators from the University of Montreal studied potential predictors of epilepsy in young patients with Sturge-Weber syndrome (SWS).
Csaba Juhász
doaj   +2 more sources

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, Rahul Kumar Gupta, Ashwani Tandon   +2 more
doaj   +1 more source