Results 21 to 30 of about 3,465 (171)
Surgical treatment of the patient with Sturge-Weber syndrome - a case report
Journal of Education, Health and Sport, 2017 Vascular malformations associated with genetic syndromes lead to dysfunction of human body organs by blood supply impairment. Disorders in the structure of blood vessels walls result in developing pathological lesions called hemangiomas.
Adrian Gnatek +2 more
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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 +4 more
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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 +3 more
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Nepal Journal of Neuroscience, 2019 Sturge-weber syndrome is a type of neurocutaneous syndrome/ neurooculo cutaneous/ phakomatoses that is characterized by facial capillary Port Wine stain, leptomeningealangioma and glaucoma with a incidence of 1 per 20-50,000 live births.
Yam Bahadur Roka
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Epilepsia Open, EarlyView.Abstract Objective Epilepsy affects approximately 50 million people worldwide and, although primarily attributed to neuronal dysfunction, increasing evidence highlights a critical role of glial cells, particularly astrocytes, in the pathophysiological mechanisms.
Chiara Lötzsch +5 more
wiley +1 more source
Sturge-Weber syndrome with ocular involvement [PDF]
Revista Brasileira de OftalmologiaSturge-Weber syndrome is a rare sporadic and congenital neurocutaneous disease characterized primarily by the presence of cutaneous and extracutaneous capillary malformations.
Oueslati Yassin +5 more
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Headache: The Journal of Head and Face Pain, EarlyView.Abstract Objective To present a practical, evidence‐based framework for the management of headache disorders in pediatric patients with prior stroke or underlying cerebral vascular lesions, with particular attention to safety and efficacy of pharmacologic and non‐pharmacologic therapies.
Allison C. Hyland +7 more
wiley +1 more source
Double trouble: Bilateral cerebral involvement in Sturge-Weber syndrome
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 +2 more
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Journal of Intellectual Disability Research, EarlyView.ABSTRACT Background Healthcare decision‐making for individuals with rare genetic neurodevelopmental disorders associated with intellectual disabilities can be complex and value‐laden, in which parents often play a central role. To ensure that clinical practice guideline recommendations align with the perspectives of parents, it is essential to ...
Mirthe J. Klein Haneveld +6 more
wiley +1 more source
Anaesthesia and the Sturge-Weber syndrome [PDF]
Canadian Journal of Anaesthesia, 1994 We report a series of 13 patients with Sturge-Weber syndrome anaesthetised on 17 occasions. Anaesthesia management varied depending on the clinical manifestations which ranged from localized, superficial skin lesions to extensive systemic involvement. These patients tolerate anaesthesia well but anaesthetic management includes evaluation for associated
R K, Batra +3 more
openaire +2 more sources