A Rare Case of Incidentally Detected Sturge-Weber Syndrome: a Case Report and Review of the Current Surgical Procedures

2019 ◽  
Vol 1 (9) ◽  
pp. 655-658
Author(s):  
Moawia Bushra Gameraddin ◽  
Kamal Dahan ◽  
Fathelrehman Alagab ◽  
Mariam Khojali
Keyword(s):  
Case Report ◽  
Surgical Procedures ◽  
Rare Case ◽  
Weber Syndrome ◽  
Sturge Weber Syndrome

scholarly journals Bilateral Sturge Weber Syndrome- a rare case report

2013 ◽  
Vol 5 (1) ◽  
pp. 129-132 ◽  
Author(s):  
P Singh ◽  
S Singh
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Unusual Case ◽  
The Other ◽  
Advanced Stage ◽  
Weber Syndrome ◽  
Rare Case Report ◽  
The Face ◽  
Bilateral Condition ◽  
Sturge Weber Syndrome

Background: Sturge-Weber syndrome is a rare congenital neuro- oculo- cutaneous disorder. Objective: To report a very rare unusual case of bilateral manifestation of Sturge Weber syndrome. Case: We report an unusual case of a 17-year-old female with advanced stage of bilateral glaucoma associated with facial nevus extending to the other half of the face as well and bilateral intracranial calcification. Conclusion: Sturge -Weber syndrome can manifest as a bilateral condition. Nepal J Ophthalmol 2013; 5(9):129-132 DOI: http://dx.doi.org/10.3126/nepjoph.v5i1.7841

scholarly journals Sturge-Weber Syndrome– A Rare Case Report

2014 ◽  
Vol 13 (5) ◽  
pp. 39-41
Author(s):  
Divyank Pathak ◽  
◽  
Dhananjay.Y Shrikhande ◽  
Nilesh Maniya ◽  
Somdeepak Reddy ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Weber Syndrome ◽  
Rare Case Report ◽  
Sturge Weber Syndrome

scholarly journals A Rare Case of Encephalotrigeminal Angiomatosis: A Case Report

2017 ◽  
Vol 7 (1) ◽  
pp. 13
Author(s):  
Lisa Elizabeth Jacob ◽  
Anuna Laila Mathew ◽  
Omal Pattali Mohanan ◽  
Thomas Abraham ◽  
Jerin Thomas ◽  
...  
Keyword(s):  
Case Report ◽  
Health Care Professionals ◽  
Rare Case ◽  
Dental Treatment ◽  
Disease Process ◽  
Adequate Knowledge ◽  
Weber Syndrome ◽  
Native Speakers Of English ◽  
Sturge Weber Syndrome ◽  
The Right

Aim: Sturge–Weber Syndrome, also known as encephalotrigeminal angiomatosis, is an uncommon, nonhereditary developmental anomaly. Methodology: A 48-year-old woman presented for routine dental treatment. She had a history of seizures and had a port wine stain on the right side of her face, which followed the distribution of the trigeminal nerve. Skull radiographs revealed “tram-track” calcifications. Conclusions: The early diagnosis of Sturge–Weber Syndrome requires a multidisciplinary approach. Oral health care professionals need adequate knowledge and understanding of the disease process to help diagnose and treat these patients.  How to cite this article: Jacob LE, Mathew AL, Omal PM, Abraham T, Thomas J, Varghese S. A Rare Case of Encephalotrigeminal Angiomatosis – A Case Report Int Dent Res 2017;7:13-6. Linguistic Revision: The English in this manuscript has been checked by at least two professional editors, both native speakers of English.

71. Sturge–Weber syndrome + cortical dysplasia. A dual pathology case report

2016 ◽  
Vol 127 (9) ◽  
pp. e319
Author(s):  
Areli Rosario Suarez-Roman ◽  
Enoe Cruz-Martinez ◽  
Yokary Amor Mellado-Ortiz ◽  
Ernesto Ramirez-Navarrete ◽  
Paul Shkurovich-Bialik
Keyword(s):  
Case Report ◽  
Cortical Dysplasia ◽  
Dual Pathology ◽  
Weber Syndrome ◽  
Sturge Weber Syndrome

STURGE WEBER SYNDROME- A RARE CASE REPORT ORIGINAL

2021 ◽  
pp. 4-5
Author(s):  
Om Prakash Singh ◽  
Vikas Kumar ◽  
Pushp Kant Tiwari
Keyword(s):  
Rare Case ◽  
Signs And Symptoms ◽  
Port Wine ◽  
Occipital Area ◽  
Weber Syndrome ◽  
Rare Case Report ◽  
The Face ◽  
Sturge Weber Syndrome ◽  
The Brain ◽  
Embryonic Vessels

Sturge-Weber Syndrome (SWS) is one of the encephalotrigeminal angiomatosis and one of the important segmental vascular neurocutaneous disorders .The occurrence is not very uncommon and the prevalence is 1:20000 to 1:50000.(1) SWS occurs due to the presence of residual embryonic vessels . The various signs and symptoms include capillary malformation in the face a port wine birthmark and similar malformation in the brain involving leptomeniges as well as blood vessels of the eye causing glaucoma. The patient presents with seizures , hemiparesis and stroke like symptoms, headaches and developmental delay.(2) The imaging nding in SWS children is the calcication in the parietal and occipital area of the brain. The EEG ndings in SWS are the attenuation and the excess of slow activities.We are presenting here a rare case of , a fourteen year old male child who presented to our emergency department with status epilepticus. The aim of presenting this case is to share the classical presentation and the challenges involved in the management

Anesthesia for a Sturge-Weber Syndrome Patient with Severe Facial Hemangioma: A case report

2006 ◽  
Vol 51 (3) ◽  
pp. 371
Author(s):  
Kyu Don Chung ◽  
Youn Suk Son ◽  
Sang Hyun Hong ◽  
Hyun Sook Cho
Keyword(s):  
Case Report ◽  
Syndrome Patient ◽  
Weber Syndrome ◽  
Sturge Weber Syndrome

Sturge-Weber Syndrome with Bipolar Presentation: A Case Report

2016 ◽  
Vol 11 (3) ◽  
Author(s):  
Zahra Mirsepassi ◽  
Fatemeh Mohammadian ◽  
Elham Hakki ◽  
Behrang Shadloo
Keyword(s):  
Case Report ◽  
Weber Syndrome ◽  
Sturge Weber Syndrome

P38.5 Case report – Status epilepticus and Sturge–Weber Syndrome

2006 ◽  
Vol 117 ◽  
pp. 1-2
Author(s):  
A. Arsovska ◽  
A. Popovski ◽  
Z. Arsovski
Keyword(s):  
Case Report ◽  
Status Epilepticus ◽  
Weber Syndrome ◽  
Sturge Weber Syndrome
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