Results 51 to 60 of about 3,465 (171)

Analysis of Sturge–Weber syndrome: A retrospective study of multiple associated variables

Neurología (English Edition), 2017
Introduction: Sturge–Weber syndrome is a congenital vascular disorder characterised by facial capillary malformation (port-wine stain) associated with venous and capillary malformations in the brain and eye. Neurological symptoms and alterations in other
A.I. Maraña Pérez, M.L. Ruiz-Falcó Rojas, V. Puertas Martín, J. Domínguez Carral, I. Carreras Sáez, A. Duat Rodríguez, V. Sánchez González   +6 more
doaj   +1 more source

Population‐Based Cohort Study for Development of National Retinopathy of Prematurity Screening Criteria

Acta Paediatrica, Volume 115, Issue 3, Page 671-678, March 2026.
ABSTRACT Aim Screening criteria for retinopathy of prematurity (ROP) vary among countries. Early detection of ROP and minimising the burden of screening are important. Methods We analysed data from very preterm infants born in Switzerland between 2006 and 2022.
R. Gerull, C. Sanchez, A. Atkinson, M. Schuler‐Barazzoni, M. Adams, F. Barcos Munoz, C. Gerth‐Kahlert, S. M. Schulzke, on behalf of the Swiss Neonatal Network, Ph. Meyer, L. Eisenhut, M. Bryant, A. Kidszun, T. Riedel, M. Gebauer, B. Rogdo, B. Wagner, R. E. Pfister, J.‐F. Tolsa, J. Schneider, M. Stocker, P. Gessler, B. Laubscher, J. Llor, A. Malzacher, A. Birkenmaier, L. Hegi, V. Bernet, M. Tomaske, D. Bassler, V. Cannizzaro, C. Hagmann   +31 more
wiley   +1 more source

The epileptologist's perspective of focal cortical dysplasia type 3: From concept to management

Epilepsia, Volume 67, Issue 3, Page 1017-1031, March 2026.
Abstract The recent International League Against Epilepsy (ILAE) official and updated classification of focal cortical dysplasia (FCD) includes a third type—FCD type 3—characterized by architectural abnormalities (cortical dyslamination) associated with another “principal” lesion: hippocampal sclerosis (HS), developmental tumors, vascular malformations,
André Palmini, Francine Oliveira, Eliseu Paglioli, Harvey Sarnat, Ricardo Paganin, Ricardo Soder, William Martins, Rafael Paglioli, Thomas Frigeri, Fernanda Schuh, Vicenzo Zarpellon   +10 more
wiley   +1 more source

Does Early Laser Treatment of Capillary Malformations Lead to More Favorable Outcomes?

The Laryngoscope, Volume 136, Issue 7, Page 2854-2855, July 2026.
Larkin Harris, Reema Padia
wiley   +1 more source

Case Report of Rasmussen's Encephalitis With a Decade of Refractory Epilepsy and Hemispheric Atrophy

Clinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT Rasmussen's encephalitis (RE) is a rare, chronic inflammatory neurological disorder affecting one cerebral hemisphere and presenting with drug‐resistant epilepsy, progressive hemiparesis, and cognitive decline. This case report describes the clinical course and management of a 21‐year‐old patient with refractory epilepsy and progressive ...
Sajjad Al‐Badri, Aditya Duhan, Rania H. Al‐Taie, Abbas Hamza Abbas, Ayah Abdulgadir, Ibrahim Khalil, Zaryab Bacha, Noran Al‐Gizey   +7 more
wiley   +1 more source

Sturge-Weber Syndrome: A Review

Actas Dermo-Sifiliográficas (English Edition), 2017
Sturge-Weber syndrome is a sporadic congenital neurocutaneous disorder caused by a somatic activating mutation in GNAQ; it affects 1 in every 20,000 to 50,000 newborns. It is characterized by a facial Port-wine stain, leptomeningeal angiomatosis, and glaucoma.
E, Higueros, E, Roe, E, Granell, E, Baselga   +3 more
openaire   +2 more sources

Dyke‐Davidoff‐Masson Syndrome: A Case of Unilateral Cerebral Atrophy and Seizure Disorder

Clinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT Dyke‐Davidoff‐Masson syndrome (DDMS) is an infrequently occurring neurological entity characterized by cerebral hemiatrophy and a collection of cognitive, motor and seizure‐related symptoms. We describe the case of an 18‐year‐old male with a long‐standing history of generalized tonic–clonic seizures following a significant fall at the age of 4.
Wasfa Shafiq, Hafiza Manahil Majeed, Hamza Hafeez Farooqi, Muhammad Waqar Khaliq, Danish Ali Chohan, Awais Mushtaq, Ali Gohar, Muhammad Husnain Ahmad   +7 more
wiley   +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

The Phakomatosis (Neurocutaneous Syndromes): Sturge-Weber Syndrome

مجله دانشکده پزشکی اصفهان, 2008
Neurocutaneous syndromes or phakomatosis are inherited or sporadic conditions that feature lesions of both skin and nervous system. Sturge-weber syndrome (SWS) is characterized by a facial cutaneaous angioma (port-wine nevus) and an associated ...
Ahmad Chitsaz
doaj  

Intelligent Supportive System for People with Profound Intellectual and Multiple Disabilities

Advanced Intelligent Systems, Volume 8, Issue 1, January 2026.
A holistic INSENSION system is developed—a novel intelligent decision support system leveraging state‐of‐the‐art noninvasive audio‐visual sensor technologies together with machine learning algorithms and expert knowledge, to detect and interpret behaviors and communications (nonverbal signals—NVSs) of people with PIMD in challenging real‐world ...
Gašper Slapničar, Michał Kosiedowski, Arkadiusz Radziuk, Erik Dovgan, Torsten Hammann, Meike Engelhardt, Christin Kupitz, Carmen Campomanes‐Alvarez, Dorota Janczewska, Peter Zentel, Mitja Luštrek   +10 more
wiley   +1 more source