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Sturge–Weber syndrome and glaucoma
Sturge–Weber syndrome (SWS) is a neurocutaneous syndrome characterized by capillary venous malformations in the skin, eye, and brain with the occurrence of angiomas of the face, choroid, and leptomeninges.
Sambavi Anbuselvan +1 more
doaj +3 more sources
Retinal Vascular Density and Vessel Diameter in Sturge-Weber Syndrome Assessed by OCT-Angiography. [PDF]
Longo R +6 more
europepmc +3 more sources
Sturge–Weber syndrome is often associated with different kinds of extraoral and intraoral manifestations, among which gingival overgrowth is one of the most common oral manifestations appreciated in the population. These oral manifestations can certainly
Sonia V Shinde, Neeta V Bhavsar
doaj +2 more sources
A Rare Case of Coexistence: Discoid Lupus Erythematosus and Sturge-Weber Syndrome. [PDF]
ABSTRACT This rare coexistence of Sturge–Weber Syndrome (SWS) and discoid lupus erythematosus (DLE) presents unique diagnostic and therapeutic challenges. It highlights potential shared environmental triggers and overlapping inflammatory mechanisms, underscoring the need for a multidisciplinary approach to management.
Efazati A +4 more
europepmc +2 more sources
A Case of Refractory Childhood Glaucoma Associated With Sturge-Weber Syndrome Treated With Baerveldt Glaucoma Implant. [PDF]
We reported the clinical course of refractory childhood glaucoma associated with Sturge–Weber syndrome (SWS) treated with Baerveldt glaucoma implant (BGI). The patient was a 14‐year‐old male diagnosed with SWS after birth. He had previously undergone four trabeculotomies for glaucoma and vitrectomy for submacular hemorrhage from a diffuse choroidal ...
Imamura W +8 more
europepmc +2 more sources
Successful treatment of glaucoma in Sturge-Weber syndrome using PreserFlo™ microshunt with intraluminal stenting: a case report. [PDF]
Inami H, Tomita R, Yuki K.
europepmc +2 more sources
Hemispherotomy for drug-resistant epilepsy in bilateral Sturge-Weber syndrome: illustrative cases. [PDF]
Hidalgo ET +9 more
europepmc +3 more sources
A Case of Congenital Glaucoma in a 5-Year-Old Patient With Sturge–Weber Syndrome and Oculodermal Melanocytosis [PDF]
Conclusions: It is possible to achieve intraocular pressure control in a patient with congenital glaucoma associated with Sturge–Weber syndrome and oculodermal melanocytosis using staged Ahmed tube insertion.
Param Shukla, Miriam Habiel
doaj +2 more sources
Sturge-Weber syndrome (SWS) is a neurocutaneous syndrome, characterized by the association of facial port-wine hemangiomas in the trigeminal nerve distribution area, with vascular malformation(s) of the brain (leptomeningeal angioma) with or without glaucoma.
Chen, Ling +4 more
openaire +4 more sources
Background Sturge-Weber syndrome is a disorder marked by a distinctive facial capillary malformation, neurological abnormalities, and ocular abnormalities such as glaucoma and choroidal hemangioma.
Zhengping Hu +3 more
doaj +1 more source

