Results 41 to 50 of about 1,569,833 (157)

Sturge-Weber Syndrome: Altered Blood Vessel Fibronectin Expression and Morphology

, 2005
Sturge-Weber syndrome presents with vascular malformations of the brain, skin, and eye. Fibronectin has potent effects on angiogenesis, vessel remodeling, and vessel innervation density. To determine fibronectin expression in the blood vessels of Sturge-
Catherine J. C. Weisz, Ellen J. Hess, Bridget H. Highet, Richard L. Skolasky, Carlos A. Pardo, Anne M. Comi   +5 more
core   +1 more source

Bloom Syndrome Presenting With Early‐Onset Myelodysplastic Syndrome and Triple Overlapping Vascular Neurocutaneous Phenotypes: A Case Report

Clinical Case Reports, Volume 14, Issue 7, July 2026.
ABSTRACT Bloom syndrome is a rare autosomal recessive chromosomal instability disorder characterized by growth deficiency and early‐onset malignancies, and its coexistence with multiple vascular neurocutaneous syndromes is exceptionally uncommon. We report an 8‐year‐old girl who presented with severe growth failure and persistent pancytopenia.
Elham Shahgholi, Nahid Khosroshahi, Sara Sadeghi   +2 more
wiley   +1 more source

Triple pathology in a patient with uncontrolled epilepsy: a case report

Journal of Medical Case Reports
Background Sturge–Weber syndrome is an uncommon neurocutaneous disorder with characteristic vascular lesions, leptomeningeal angiomas, and facial nevi. Seizureis the most prevalent neurological sign of Sturge–Weber syndrome and complications related to ...
Sara Ranji, Behnam Akbari, Melika Javani, Aidin Taghilou, Abbas Tafakhori, Saeideh Salehizadeh, Hoda Naghshineh   +6 more
doaj   +1 more source

Intracerebral hemorrhage in Sturge Weber Syndrome: A case report [PDF]

Romanian Journal of Neurology
Background. Encephalotrigeminal angiomatosis also called Sturge Weber Syndrome (SWS) is neurocutaneous abnormality with angioma affecting the leptomeninges and the face skin, commonly in the eyes and maxillary distribution of trigeminal nerve.
Rizaldy Taslim Pinzon, I Gusti Agung Oka Pratama   +1 more
doaj   +1 more source

Surgical treatment of glaucoma with filtration bleb activation of a patient with Sturge — Weber syndrome: a clinical case

Российский офтальмологический журнал, 2022
Purpose: to describe surgical treatment of glaucoma of a patient with Sturge — Weber — Krabbe syndrome. We present a clinical case of a patient with Sturge — Weber — Krabbe syndrome who sought assistance with us due to secondary stage III glaucoma with ...
T. N. Savranova, V. U. Rozukulov, A. F. Yusupov, D. A. Asadov, S. S. Saidzhonov   +4 more
doaj   +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, V, Gulaya, R, Madan, A, Trikha   +3 more
openaire   +2 more sources

Familial p.(Ala73Thr) Variant in GNB2 Associated With Mild Neurodevelopmental Features and Pilocytic Astrocytoma

Clinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Pathogenic variants in GNB2 have been associated with a neurodevelopmental disorder that includes global developmental delays and intellectual disability, hypotonia, increased risk for seizures, heart and renal anomalies, and characteristic facial features.
Megan Glassford, Caroline Jennings, Anne Slavotinek   +2 more
wiley   +1 more source

A case of Exudative Retinal Detachment after Fistulizing Antiglaucoma Surgery in a Patient with Sturge — Weber Syndrome

Oftalʹmologiâ
A clinical case of exudative retinal detachment after trabeculectomy for secondary glaucoma with Sturge-Weber syndrome is presented. A 50-year-old female patient with Sturge-Weber syndrome sought help for secondary glaucoma with elevated intraocular ...
S. Yu. Petrov, T. N. Kiseleva, K. A. Ramazanova, A. V. Starostina, O. I. Markelova   +4 more
doaj   +1 more source

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

Prosthodontic and Occlusal Management of a Patient With Facial Port‐Wine Stains: A Case Report

Clinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT This study aims to present the prosthetic rehabilitation of a patient affected by Port‐Wine Stain (PWS), a condition involving intraoral tissues that may pose challenges to removable prosthodontic treatment due to altered mucosal resiliency, pronounced hypersensitivity, and vascular fragility.
Ana‐Maria Condor, Daniela Cornelia Condor, Andreea Kui, Simona Iacob, Alexandra Tărchilă, Smaranda Buduru, Andrea Chisnoiu   +6 more
wiley   +1 more source