Results 61 to 70 of about 3,465 (171)

Beyond Treatment: The Strategy of Nonintervention in Choroidal Hemangioma

Clinical Case Reports, Volume 14, Issue 1, January 2026.
ABSTRACT The circumscribed choroidal hemangioma (CCH) is a benign congenital eye tumor whose etiology is not clear. A 41‐year‐old female patient came with a 2‐year history of slowly progressive deteriorating vision in her right eye. In the left eye, the best‐corrected visual acuity (BCVA) was 6/6, and counting fingers at 1 m in the right eye.
Humdan Khan, Muhammad Shaheer Bin Faheem, Hurmat Fatima, Asfandyar Asghar, Ahmed Ali Khan, Muhammad Rehan Zahid, Syed Tawassul Hassan, Izzah Shakkel, Muhammad Idrees Khan   +8 more
wiley   +1 more source

Anaesthetic Management of A Patient with Sturge-Weber Syndrome Undergoing Oophorectomy

Indian Journal of Anaesthesia, 2009
The Sturge-Weber Syndrome (SWS) is a neurocutaneous disorder characterized by leptomeningeal and facial angiomas, neurologic and ocular manifestations. We report a case of oophorectomy for ovarian dermoid in a 14 year -old girl who was a diagnosed case ...
Manju Gandhi, Hemlata Iyer, Herman Sehmbi, Kavita Datir   +3 more
doaj  

Spectrum of CT and MR findings in Sturge-Weber syndrome: A case report

Medical Journal of Dr. D.Y. Patil University, 2014
Sturge-Weber syndrome is an uncommon, sporadically occurring neurocutaneous syndrome characterized by port wine stain (facial nevus flammeus), congenital glaucoma, and anomalous leptomeningeal angiomatous malformation.
Pallavi J Agrawal, Amit T Kharat, Rajesh Kuber, Sunita Shewale   +3 more
doaj   +1 more source

Sturge–Weber syndrome [PDF]

QJM: An International Journal of Medicine, 2018
T-H, Ho, F-C, Yang, J-C, Lin, C-H, Hsu, J-T, Lee   +4 more
openaire   +3 more sources

Sturge-Weber Syndrome : A Report Of Three Cases

Indian Journal of Dermatology, 2001
Three cases of Sturge â€" Weber syndrome are being reported. All our cases had incomplete form of Sturge- Weber syndrome. They had cutaneous facial angiomas and leptomeningeal agiomas evidenced by central nervous system manifestations (
Jeevankumar B, Mohan Thappa Devinder
doaj  

Você conhece esta síndrome? Do you know this syndrome?

Anais Brasileiros de Dermatologia, 2008
A síndrome de Sturge-Weber é doença congênita esporádica composta por malformação capilar dérmica facial na área do ramo oftálmico do nervo trigêmio, associada a malformações vasculares das leptomeninges e dos olhos.
Maria Ester Massara Café, Rogério da Costa Rodrigues, Agnella Massara Viggiano   +2 more
doaj   +1 more source

Predicting and Preventing Epilepsy in Sturge-Weber Syndrome?

Pediatric Neurology Briefs, 2016
Investigators from the University of Montreal studied potential predictors of epilepsy in young patients with Sturge-Weber syndrome (SWS).
Csaba Juhász
doaj   +1 more source

Phakomatosis Pigmentovascularis Coexisting with a Variant of Sturge Weber Syndrome - A Rare Occurrence

Delhi Journal of Ophthalmology, 2019
The spectrum of phacomatoses is wide and they share common pathophysiological changes. The various entities widely studied and being reported are Sturge Weber Syndrome (SWS), Klippel Trenaunay Syndrome and Phakomatosis Pigmentovascularis (PPV).
Priyanka Singh, Nayana A. Potdar, Ankita Patil, Pritam K. Mohite, Chhaya A. Shinde, Pooja Bandivadekar   +5 more
doaj   +1 more source

Intraoral capillary hemangioma in Sturge–Weber syndrome - A rare case report and its periodontal management

Journal of Indian Society of Periodontology
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   +1 more source

Neurocutaneous Syndromes and Epilepsy

Archives of Epilepsy, 2016
Objectives:Neurocutaneous syndromes are genetic diseases that affect the nervous system and the skin. Epileptic seizures are seen with variable frequency.
Abidin ERDAL, Aylin BİCAN DEMİR, İpek MİDİ, Yasemin BİÇER GÖMCELİ, Gülnihal KUTLU, S. Naz YENİ, İbrahim BORA   +6 more
doaj   +1 more source