Results 51 to 60 of about 1,569,833 (157)

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

Síndrome de Sturge-Weber tratado con láser de colorante pulsado [PDF]

, 2019
The Sturge-Weber syndrome is a sporadic, congenital, neurocutaneous disorder. Its clinical manifestations include facial capillary malformation, leptomeningeal angioma, and angiomatous choroidal lesions in the eye predisposing to glaucoma.
Vásquez, Luz Adriana, Arredondo, María Isabel, Toro, Ana Milena, Montes, Ana Milena, Molina, Verónica, Arroyave, Juan Esteban   +5 more
core  

Sturge-Weber syndrome. A case report

, 2017
Sturge-Weber syndrome is a rare disorder that occurs sporadically with a frequency of 1:50,000. It is characterized by facial nevus, seizures, hemiparesis, intracranial calcification and mental retardation.
Humayun Iqbal Khan, Mhammad Faheem Afzal, Fariha Anjum, Tahir Javed   +3 more
core   +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

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

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

Adult Sturge Weber Syndrome : Cranial Mri and Ct Findings in Three Cases

, 2017
Sturge Weber Syndrome (SWS), also known as encephalotrigeminal angiomatosis, is a rare neurocutaneous syndrome which is characterized by a classical clinical triad of Port-wine stain of the face, epilepsy and glaucoma.
Deniz Sözmen Cılız, Gözde Tufan, Mehtap Çavușoğlu, Bülent Sakman, Semra Duran   +4 more
core   +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

Clinical Validation of a Fast MRI Method to Evaluate Brain Vascular and Parenchymal Abnormalities in Sturge‐Weber Syndrome

Journal of Magnetic Resonance Imaging, Volume 63, Issue 5, Page 1270-1281, May 2026.
ABSTRACT Background Sturge‐Weber syndrome (SWS) is a rare neurocutaneous disorder associated with venous capillary malformations, atrophy, and calcifications. Longitudinal imaging is limited by risks of sedation and gadolinium exposure in children.
Scotty G. McKay, Yongsheng Chen, E. Mark Haacke, Yang Xuan, Aimee F. Luat, Csaba Juhász   +5 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