Results 41 to 50 of about 3,465 (171)

Análisis del síndrome de Sturge-Weber: estudio retrospectivo de múltiples variables asociadas

Neurología, 2017
Resumen: Introducción: El síndrome de Sturge-Weber es un trastorno vascular congénito caracterizado por una malformación facial capilar (mancha en vino de Oporto) asociada a malformaciones venosas y capilares en el cerebro y en el ojo.
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

Development and Retrospective Application of Novel Outcome Measure: Sturge–Weber Syndrome Acute Crisis (SWAC) Index

Annals of the Child Neurology Society, Volume 4, Issue 2, Page 132-139, June 2026.
ABSTRACT Objective Sturge–Weber syndrome (SWS) symptoms frequently overlap in neurological acute crises (ACs) presenting with seizures, stroke‐like episodes (SLE), and headaches. Recent efforts to develop a prospective drug trial highlighted the need for a new outcome measure capable of quantifying these symptoms during an SWS AC.
Kieran D. McKenney, Luther G. Kalb, Adrienne M. Hammill, Anne M. Comi   +3 more
wiley   +1 more source

Angiodysplastic Sturge Weber syndrome [PDF]

BMJ Case Reports, 2018
A 3-year-old boy presented with global developmental delay, abnormal craniofacial growth and left focal seizures since infancy. He was the first child of a non-consanguineous couple with unremarkable perinatal period. Family history was non-contributory.
Ananthanaryanan, Kasinathan, Arushi Gahlot, Saini, Sameer, Vyas, Pratibha, Singhi   +3 more
openaire   +2 more sources

Bilateral Ocular and Facial with Unilateral Intracranial Involvement In Sturge Weber Syndrome: A Case Report and Review of Literature

Delhi Journal of Ophthalmology, 2017
The Sturge-Weber syndrome (SWS) is a rare congenital disorder involving the eye in the form of glaucoma and choroidal hemangioma, facial skin in the form of port wine stain, usually in the distribution of ophthalmic division of the trigeminal nerve, and ...
Mihika Dube, Rashmi Kujur, Swati Prajapati   +2 more
doaj   +1 more source

Steroids for Drug‐Resistant Seizures and Prolonged Stroke‐Like Episode in a Patient With Sturge–Weber Syndrome: A Case Report

Annals of the Child Neurology Society, Volume 4, Issue 2, Page 159-166, June 2026.
ABSTRACT Introduction Sturge–Weber syndrome (SWS) brain involvement has been associated with impairments in the blood–brain barrier (BBB) and microglial activation within involved cortical regions. Acute neurological crises, including seizures, stroke‐like episodes, and/or significant headaches, are common in these patients.
Brenna N. Keam, Fabiola A. Morales‐Vias, Siddharth S. Gupta, Doris D. Lin, Anne M. Comi   +4 more
wiley   +1 more source

63. Pulmonary atresia with intact ventricular septum, associated with intracranial calcifications and left parietal hemangioma (Sturge–Weber Syndrome)

Journal of the Saudi Heart Association, 2015
Neurocutaneous disorders are characterized by skin lesions (port wine stain, hypopigmented patches) associated with intracranial features (ipsilateral leptomeningeal angiomas, intracranial calcifications and subsequent seizures).
Muna Babiker, Abdulrahman S. Almoukirish, Mohammed Omar Galal   +2 more
doaj   +1 more source

Sturge–Weber Syndrome with Bilateral Port-Wine Stain

Case Reports in Pediatrics, 2022
Sturge–Weber syndrome is a rare congenital neurocutaneous disorder characterized by dermatological, ophthalmological, and neurological manifestations. It occurs due to abnormal persistence of embryonic vascular plexus.
Bishnu Deep Pathak, Shriya Sharma, Aakriti Adhikari, Nabin Simkhada, Bhuwan Ghimire, Nirjala Aryal   +5 more
doaj   +1 more source

Head and Neck Clinical Signs Associated With Diseases: A Scoping Review

Special Care in Dentistry, Volume 46, Issue 3, May/June 2026.
ABSTRACT Objective Clinical signs observed during head and neck examination offer important diagnostic clues. This scoping review aimed to identify key clinical signs in this region associated with diseases and syndromes and to map them according to their location. Methods An electronic literature search was performed in five databases (Embase, LILACS,
Helena Miguel Cotter, Mateus José Dutra, Gustavo Davi Rabelo, Ana Carolina Prado Ribeiro, Marcio Ajudarte Lopes, Márcio Diniz‐Freitas, Luiz Paulo Kowalski, Alan Roger Santos‐Silva, Caique Mariano Pedroso   +8 more
wiley   +1 more source

Klippel–Trenaunay and Sturge–Weber Overlap Syndrome with KRAS and GNAQ mutations

Annals of Clinical and Translational Neurology, 2020
Patients with combined phenotypes of Sturge–Weber syndrome and Klippel–Trenaunay syndrome have been reported, though the underlying genetic spectrum in these individuals remains to be elucidated.
Ruojie He, Songjie Liao, Xiaoli Yao, Ruxun Huang, Jinsheng Zeng, Jian Zhang, Jian Yu   +6 more
doaj   +1 more source

An Infant With Phakomatosis Pigmentovascularis Complicated by Multisystem Damage: Elaborate Care Leads to a Positive Outcome

Clinical Case Reports, Volume 14, Issue 3, March 2026.
ABSTRACT This report highlights the value of multidisciplinary collaboration, personalized care, dynamic monitoring of seizure activity, and innovative skin management in a 2‐month‐old with Phakomatosis Pigmentovascularis. In parallel, the nursing team implemented a multidimensional “medical–social–psychological” support model, providing psychological ...
Kaimin Chen, Xiaoxia Huang, Xin Jin, Lilan He, Mingzhu He, Wenli Shen, Yuling Zheng   +6 more
wiley   +1 more source