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Page 1
Updates on Sturge-Weber Syndrome.
Yeom S, Comi AM. Yeom S, et al. Stroke. 2022 Dec;53(12):3769-3779. doi: 10.1161/STROKEAHA.122.038585. Epub 2022 Oct 20. Stroke. 2022. PMID: 36263782 Free PMC article. Review.
Sturge-Weber syndrome (SWS) is a rare, noninherited neurovascular disorder characterized by abnormal vasculature in the brain, skin, and eye. ...This review focuses on the latest progress in the field of research for Sturge-Weber syndrome
Sturge-Weber syndrome (SWS) is a rare, noninherited neurovascular disorder characterized by abnormal vasculature in the
Sturge-Weber Syndrome: A Review.
Higueros E, Roe E, Granell E, Baselga E. Higueros E, et al. Actas Dermosifiliogr. 2017 Jun;108(5):407-417. doi: 10.1016/j.ad.2016.09.022. Epub 2017 Jan 23. Actas Dermosifiliogr. 2017. PMID: 28126187 Free article. Review. English, Spanish.
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. ...Neuroimaging studies show leptomeningeal angiomatosis, supporting diagnosis. Standard t
Sturge-Weber syndrome is a sporadic congenital neurocutaneous disorder caused by a somatic activating mutation in GNAQ;
Sturge-Weber syndrome.
Comi AM. Comi AM. Handb Clin Neurol. 2015;132:157-68. doi: 10.1016/B978-0-444-62702-5.00011-1. Handb Clin Neurol. 2015. PMID: 26564078 Review.
Sturge-Weber syndrome is the third most common neurocutaneous disorder, after neurofibromatosis and tuberous sclerosis, and impacts approximately 1 in 20000 live births. Sturge-Weber syndrome is not inherited, but rather occurs exclusivel
Sturge-Weber syndrome is the third most common neurocutaneous disorder, after neurofibromatosis and tuberous sclerosis,
Consensus Statement for the Management and Treatment of Sturge-Weber Syndrome: Neurology, Neuroimaging, and Ophthalmology Recommendations.
Sabeti S, Ball KL, Bhattacharya SK, Bitrian E, Blieden LS, Brandt JD, Burkhart C, Chugani HT, Falchek SJ, Jain BG, Juhasz C, Loeb JA, Luat A, Pinto A, Segal E, Salvin J, Kelly KM. Sabeti S, et al. Pediatr Neurol. 2021 Aug;121:59-66. doi: 10.1016/j.pediatrneurol.2021.04.013. Epub 2021 May 6. Pediatr Neurol. 2021. PMID: 34153815 Free PMC article.
BACKGROUND: Sturge-Weber syndrome (SWS) is a sporadic, neurocutaneous syndrome involving the skin, brain, and eyes. ...
BACKGROUND: Sturge-Weber syndrome (SWS) is a sporadic, neurocutaneous syndrome involving the skin, brain, and ey …
Sturge-Weber syndrome.
Ho TH, Yang FC, Lin JC, Hsu CH, Lee JT. Ho TH, et al. QJM. 2019 Apr 1;112(4):299. doi: 10.1093/qjmed/hcy246. QJM. 2019. PMID: 30357409 No abstract available.
Sturge-Weber syndrome: an update for the pediatrician.
Dingenen E, Segers D, De Maeseneer H, Van Gysel D. Dingenen E, et al. World J Pediatr. 2024 May;20(5):435-443. doi: 10.1007/s12519-024-00809-y. Epub 2024 Apr 24. World J Pediatr. 2024. PMID: 38658498 Review.
BACKGROUND: Sturge-Weber syndrome (SWS) is a rare congenital neurocutaneous disorder characterized by the simultaneous presence of both cutaneous and extracutaneous capillary malformations. ...A search of PubMed, Google Scholar and Embase was conducted, using …
BACKGROUND: Sturge-Weber syndrome (SWS) is a rare congenital neurocutaneous disorder characterized by the simultaneous …
Port-wine Birthmarks: Update on Diagnosis, Risk Assessment for Sturge-Weber Syndrome, and Management.
Poliner A, Fernandez Faith E, Blieden L, Kelly KM, Metry D. Poliner A, et al. Pediatr Rev. 2022 Sep 1;43(9):507-516. doi: 10.1542/pir.2021-005437. Pediatr Rev. 2022. PMID: 36045161 Review.
Sturge-Weber syndrome (SWS) is a neurocutaneous disorder that classically presents with a triad of vascular anomalies affecting the skin, eyes, and brain. ...
Sturge-Weber syndrome (SWS) is a neurocutaneous disorder that classically presents with a triad of vascular anomalies a
Sturge-Weber syndrome: an update on the relevant issues for neurosurgeons.
Bianchi F, Auricchio AM, Battaglia DI, Chieffo DRP, Massimi L. Bianchi F, et al. Childs Nerv Syst. 2020 Oct;36(10):2553-2570. doi: 10.1007/s00381-020-04695-3. Epub 2020 Jun 21. Childs Nerv Syst. 2020. PMID: 32564157 Review.
PURPOSE: Sturge-Weber syndrome (SWS) is a neurocutaneous facomatosis characterized by facial and leptomeningeal angioma, glaucoma, seizures, and neurological disability. ...
PURPOSE: Sturge-Weber syndrome (SWS) is a neurocutaneous facomatosis characterized by facial and leptomeningeal angioma …
Neurological Complications of Sturge-Weber Syndrome: Current Status and Unmet Needs.
Luat AF, Juhász C, Loeb JA, Chugani HT, Falchek SJ, Jain B, Greene-Roethke C, Amlie-Lefond C, Ball KL, Davis A, Pinto A. Luat AF, et al. Pediatr Neurol. 2019 Sep;98:31-38. doi: 10.1016/j.pediatrneurol.2019.05.013. Epub 2019 Jun 6. Pediatr Neurol. 2019. PMID: 31272784 Review.
OBJECTIVE: We aimed to identify the current status and major unmet needs in the management of neurological complications in Sturge-Weber syndrome. METHODS: An expert panel consisting of neurologists convened during the Sturge-Weber Foundation Cl …
OBJECTIVE: We aimed to identify the current status and major unmet needs in the management of neurological complications in Sturge- …
Sturge-Weber syndrome.
Baselga E. Baselga E. Semin Cutan Med Surg. 2004 Jun;23(2):87-98. doi: 10.1016/j.sder.2004.01.002. Semin Cutan Med Surg. 2004. PMID: 15295918 Review.
Sturge-Weber syndrome is a sporadic neurocutaneous disease characterized by facial port-wine stain, ocular abnormalities (glaucoma and choroidal hemangioma) and leptomeningeal angioma. ...Early neuroimaging features are important to recognize. Management of p
Sturge-Weber syndrome is a sporadic neurocutaneous disease characterized by facial port-wine stain, ocular abnormalitie
1,977 results