Results 91 to 100 of about 1,569,833 (157)

Neurocutaneous Syndromes and Epilepsy

Archives of Epilepsy, 2016
Objectives:Neurocutaneous syndromes are genetic diseases that affect the nervous system and the skin. Epileptic seizures are seen with variable frequency.
Abidin ERDAL, Aylin BİCAN DEMİR, İpek MİDİ, Yasemin BİÇER GÖMCELİ, Gülnihal KUTLU, S. Naz YENİ, İbrahim BORA   +6 more
doaj   +1 more source

An unusual case of acute glaucoma in Sturge-Weber syndrome

, 2015
Sturge-Weber syndrome is a phakomatosis with involvement of the eyelids, conjunctiva, choroid, and retina. Congenital glaucoma is the most common ocular complication resulting from raised episcleral venous pressure. We present an unusual case of glaucoma
MANNINO, Giuseppe, Mantelli, Flavio, LAMBIASE, ALESSANDRO, RECUPERO, Santi Maria   +3 more
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Sturge Weber Syndrome Diagnosed at Late Age, Associated with Psychiatric Complaints and Status: A Case Report

, 2018
Sturge-Weber syndrome (SWS) is a rare, sporadic neurocutaneous syndrome characterized by a usually unilateral facial port-wine stain, ipsilateral leptomeningeal angiomatosis, glaucoma, epileptic seizures that are difficult to control, and progressive ...
Eren GÖZKE, Hilal TAŞTEKİN TOZ, Boran Can SARAÇOĞLU   +2 more
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Sturge Weber Syndrome (Encephalotrigeminal Angiomatosis)

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. Optic disc is cupped due to elevated intraocular pressure. (Secondary
William F. Hoyt, MD
core   +1 more source

Sturge-Weber Syndrome: A Review of Pathophysiology, Genetics, Clinical Features, and Current Management Approache [Corrigendum]

The Application of Clinical Genetics
Sánchez-Espino LF, Ivars M, Antoñanzas J, Baselga E. Appl Clin Genet. 2023;16:63–81. It has come to our attention that there is an error in the paper title on page 63, the title “Sturge-Weber Syndrome: A Review of ...
Sánchez-Espino LF, Ivars M, Antoñanzas J, Baselga E   +3 more
doaj  

Surgical Outcome in Sturge-Weber Syndrome

, 2000
The presurgical epilepsy profile, criteria for surgery, and postoperative outcome of epilepsy were assessed in 20 patients with Sturge-Weber syndrome (SWS) consecutively admitted to the Hopital des Enfants Malades in Paris and the Montreal Neurological ...
J Gordon Millichap
core   +1 more source

Choroidal detachment with exudative retinal detachment following Ahmed valve implantation in Sturge-Weber syndrome

, 2019
Ahmed glaucoma valve implant appears to be a relatively useful drainage device in eyes with glaucoma secondary to Sturge-Weber syndrome (SWS). However, early postoperative choroidal and exudative retinal detachment may occur from a rapid expansion of the
Sadiq, A, Salam, A, Badmus, S, Sarker, BK, Hassan, Z, Mahatma, M, Rahman, M, Malek, MIA, Kabir, J, Sazzad, I, Helen, G   +10 more
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Psychopathology in Sturge-Weber Syndrome^*

, 1990
Sturge-Weber syndrome is a rare congenital disease which can impair a child's brain functions and psychosocial development. Its psychiatric aspects have been ignored in the literature.
Sing Lee
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Sturge-Weber syndrome involved frontoparietal region without facial Nevus

, 2002
Classic Sturge-Weber syndrome is characterized by a facial nevus and hamartomatous lesion in the brain. Hamartomatous lesions are usually located in the ipsilateral occipital region of the facial nevus. The other lobes may be involved.
TAŞDEMİR, Haydar Ali, DİLBER, Cengiz, Odaci, ERSAN, İNCESU, Lutfi, DAĞDEMİR, Ayhan   +4 more
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Sturge-Weber Syndrome and Related Cerebrovascular Malformation Syndromes

, 2017
Sturge-Weber syndrome is a rare disorder presenting with a capillary malformation, better known as a port-wine birthmark, on the upper face, glaucoma, and a leptomeningeal angioma.
Angela Quain, Anne M. Comi
core   +1 more source