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2,103 results

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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, …
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 …
Sturge-Weber syndrome.
Di Rocco C, Tamburrini G. Di Rocco C, et al. Childs Nerv Syst. 2006 Aug;22(8):909-21. doi: 10.1007/s00381-006-0143-2. Epub 2006 Jul 6. Childs Nerv Syst. 2006. PMID: 16823586 Review.
INTRODUCTION: Sturge-Weber syndrome (SWS) is a rare neurocutaneous syndrome the main clinical features of which are facial, mostly unilateral nevi, leptomeningeal angiomatosis, and congenital glaucoma. The interest of this syndrome for pediatric …
INTRODUCTION: Sturge-Weber syndrome (SWS) is a rare neurocutaneous syndrome the main clinical features of which …
Sturge-Weber syndrome.
Nabbout R, Juhász C. Nabbout R, et al. Handb Clin Neurol. 2013;111:315-21. doi: 10.1016/B978-0-444-52891-9.00037-3. Handb Clin Neurol. 2013. PMID: 23622182 Review.
Sturge-Weber syndrome (SWS) is a rare sporadic neurocutaneous syndrome defined by the association of a facial capillary malformation in the ophthalmic distribution of the trigeminal nerve, with ipsilateral vascular glaucoma and vascular malformation of …
Sturge-Weber syndrome (SWS) is a rare sporadic neurocutaneous syndrome defined by the association of a facial ca …
Biomarker development in Sturge-Weber syndrome.
Gupta SS, Joslyn KE, McKenney KD, Comi AM. Gupta SS, et al. J Neurodev Disord. 2025 Aug 25;17(1):50. doi: 10.1186/s11689-025-09640-6. J Neurodev Disord. 2025. PMID: 40851064 Free PMC article. Review.
Sturge-Weber Syndrome (SWS) is a congenital neurovascular disorder caused by a somatic mosaic mutation in the R183Q GNAQ gene and characterized by capillary-venous malformations of the brain, skin, and eyes. ...
Sturge-Weber Syndrome (SWS) is a congenital neurovascular disorder caused by a somatic mosaic mutation in the R183Q GNA …
[Sturge-Weber syndrome].
Maruani A. Maruani A. Presse Med. 2010 Apr;39(4):482-6. doi: 10.1016/j.lpm.2009.07.030. Epub 2010 Mar 10. Presse Med. 2010. PMID: 20219318 Review. French.
Facial port-wine stains are capillary malformations, which can reveal, very rarely, Sturge-Weber syndrome (SWS). SWS is a severe neurocutaneous syndrome, which involves a facial port-wine stain reaching the first branch of trigeminal nerve (V1), ophtha …
Facial port-wine stains are capillary malformations, which can reveal, very rarely, Sturge-Weber syndrome (SWS). SWS is …
The Sturge-Weber syndrome.
Paller AS. Paller AS. Pediatr Dermatol. 1987 Dec;4(4):300-4. doi: 10.1111/j.1525-1470.1987.tb00797.x. Pediatr Dermatol. 1987. PMID: 3328186 Review.
The Sturge-Weber syndrome is characterized by angiomas of the leptomeninges overlying the cerebral cortex in association with a facial nevus flammeus. Although frequently included with other neurocutaneous genodermatoses, the syndrome is almost always …
The Sturge-Weber syndrome is characterized by angiomas of the leptomeninges overlying the cerebral cortex in associatio …
Sturge-Weber syndrome: a review.
Thomas-Sohl KA, Vaslow DF, Maria BL. Thomas-Sohl KA, et al. Pediatr Neurol. 2004 May;30(5):303-10. doi: 10.1016/j.pediatrneurol.2003.12.015. Pediatr Neurol. 2004. PMID: 15165630 Review.
Sturge-Weber syndrome is a rare disorder that occurs with a frequency of approximately 1 per 50,000. ...The clinical course is highly variable and some children experience intractable seizures, mental retardation, and recurrent strokelike episodes. In this re …
Sturge-Weber syndrome is a rare disorder that occurs with a frequency of approximately 1 per 50,000. ...The clinical co …
2,103 results