ILAE classification and definition of epilepsy syndromes with onset in neonates and infants: Position statement by the ILAE Task Force on Nosology and Definitions

SM Zuberi, E Wirrell, E Yozawitz, JM Wilmshurst… - …, 2022 - Wiley Online Library
Abstract The International League Against Epilepsy (ILAE) Task Force on Nosology and
Definitions proposes a classification and definition of epilepsy syndromes in the neonate …

[HTML][HTML] Sturge-Weber syndrome: a review

E Higueros, E Roe, E Granell, E Baselga - Actas Dermo-Sifiliográficas …, 2017 - Elsevier
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 …

Mosaic neurocutaneous disorders and their causes

M Ruggieri, AD Praticò - Seminars in Pediatric Neurology, 2015 - Elsevier
Neurocutaneous disorders are a heterogeneous group of conditions (mainly) affecting the
skin [with pigmentary/vascular abnormalities and/or cutaneous tumours] and the central and …

Screening for Sturge‐Weber syndrome: A state‐of‐the‐art review

M Zallmann, RJ Leventer, MT Mackay… - Pediatric …, 2018 - Wiley Online Library
Infants with a high‐risk distribution of port‐wine stains are commonly screened for Sturge‐
Weber syndrome using brain magnetic resonance imaging. There is no consensus about …

Predictors of cognitive functions in children with Sturge–Weber syndrome: a longitudinal study

E Bosnyák, ME Behen, WC Guy, E Asano… - Pediatric …, 2016 - Elsevier
Abstract Background Sturge–Weber syndrome is often accompanied by seizures and
neurocognitive deterioration, although previous studies have suggested that early functional …

Sturge-Weber syndrome: an update on the relevant issues for neurosurgeons

F Bianchi, AM Auricchio, DI Battaglia, DRP Chieffo… - Child's Nervous …, 2020 - Springer
Abstract Purpose Sturge-Weber syndrome (SWS) is a neurocutaneous facomatosis
characterized by facial and leptomeningeal angioma, glaucoma, seizures, and neurological …

Seizure, Motor, and Cognitive Outcomes After Epilepsy Surgery for Patients With Sturge-Weber Syndrome: Results From a Multicenter Study

S Wang, QZ Liu, R Zhao, X Zhai, K Zhang, L Cai, S Li… - Neurology, 2024 - neurology.org
Background and Objectives Surgery is widely performed for refractory epilepsy in patients
with Sturge-Weber syndrome (SWS), but reports on its effectiveness are limited. This study …

Quantitative EEG improves prediction of Sturge-Weber syndrome in infants with port-wine birthmark

RE Gill, B Tang, L Smegal, JH Adamek… - Clinical …, 2021 - Elsevier
Objective Port-wine birthmark (PWB) is a common occurrence in the newborn, and general
pediatricians, dermatologists, and ophthalmologists are often called on to make an …

Epileptogenesis in neurocutaneous disorders with focus in Sturge Weber syndrome

A Pinto, M Sahin, PL Pearl - F1000Research, 2016 - pmc.ncbi.nlm.nih.gov
Epilepsy is a major morbidity in Sturge Weber syndrome, a segmental vascular
neurocutaneous disorder classically associated with facial angiomas, glaucoma, and …

Retrospective review of screening for Sturge‐Weber syndrome with brain magnetic resonance imaging and electroencephalography in infants with high‐risk port …

M Zallmann, MT Mackay, RJ Leventer… - Pediatric …, 2018 - Wiley Online Library
Background There is a lack of consensus regarding how best to screen children with facial
port‐wine stains for Sturge‐Weber syndrome. Many favor brain magnetic resonance …