Results 21 to 30 of about 5,302 (181)

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, Pratiksha Hada, Vikram Singh, Mamta Singh   +3 more
doaj   +1 more source

Hippocampal sclerosis in association with Sturge-weber syndrome: An intertwining of 2 epileptogenic lesions. [PDF]

Radiol Case Rep
AlAlwan MQ, Alsaad FA, Alhashem HY, Altaweel I, AlAlwan QM, Al Obaid JJ, Almohammed Ali HA.   +6 more
europepmc   +2 more sources

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   +1 more source

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, Khadim Mbacké Ndiaye, Alassane Mamadou Diop, Ibrahima Faye, Mbaye Thiam, Coumba Laobé Ndao, Sokhna Ba   +6 more
doaj   +1 more source

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

Sturge weber syndrome: A case report. [PDF]

Clin Case Rep
Karn M, Barma A, Ojha L, Bhatta S, Neupane P, Dhital K, Sharma A, Acharya S, Unika KC, Barma A, Mahato D, Rawal G.   +11 more
europepmc   +3 more sources

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, Karina Nagao, Sansão Isaac Kac, Marcelo Palis Ventura   +3 more
doaj   +1 more source

Unusual presentation of Sturge-Weber syndrome: Progressive megalencephaly with bilateral cutaneous and cortical involvement

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, Jaya Shankar Kaushik, Gurpreet Kaur, Mohd Aamir, Suvasini Sharma   +4 more
doaj   +1 more source

A Review of Sturge-Weber Syndrome Brain Involvement, Cannabidiol Treatment and Molecular Pathways. [PDF]

Molecules
Joslyn KE, Truver NF, Comi AM.
europepmc   +3 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   +1 more source