Reversible increases in cortical diffusion-weighted MR signal in a patient with Sturge–Weber syndrome and subacute hemiplegia

2011 ◽  
Vol 258 (11) ◽  
pp. 2095-2096
Author(s):  
Christopher Kobylecki ◽  
Matthew Jones ◽  
Toby Williams ◽  
Alexander Gerhard
Keyword(s):  
Diffusion Weighted ◽  
Weber Syndrome ◽  
Sturge Weber Syndrome

Sturge-Weber syndrome and multiple myeloma

1969 ◽  
Vol 100 (4) ◽  
pp. 488b-488
Author(s):  
H. O. Curth
Keyword(s):  
Multiple Myeloma ◽  
Weber Syndrome ◽  
Sturge Weber Syndrome

Outcome of infants with unilateral Sturge-Weber syndrome and early onset seizures

2000 ◽  
Vol 42 (11) ◽  
pp. 756-759 ◽  
Author(s):  
Uri Kramer ◽  
Esther Kahana ◽  
Zamir Shorer ◽  
Bruria Ben-Zeev
Keyword(s):  
Early Onset ◽  
Weber Syndrome ◽  
Sturge Weber Syndrome

scholarly journals Screening for Sturge-Weber syndrome: A state-of-the-art review

2017 ◽  
Vol 35 (1) ◽  
pp. 30-42 ◽  
Author(s):  
Michaela Zallmann ◽  
Richard J. Leventer ◽  
Mark T. Mackay ◽  
Michael Ditchfield ◽  
Philip S. Bekhor ◽  
...  
Keyword(s):  
State Of The Art ◽  
Weber Syndrome ◽  
Sturge Weber Syndrome

scholarly journals Periodontal Management of Sturge-Weber Syndrome

2013 ◽  
Vol 2013 ◽  
pp. 1-4 ◽  
Author(s):  
Butchibabu Kalakonda ◽  
Koppolu Pradeep ◽  
Ashank Mishra ◽  
Krishnanjaneya Reddy ◽  
Tupili Muralikrishna ◽  
...  
Keyword(s):  
Oral Manifestations ◽  
Port Wine Stain ◽  
Scaling And Root Planing ◽  
Port Wine ◽  
Ocular Abnormalities ◽  
Parietal Lobes ◽  
Gingival Enlargement ◽  
Weber Syndrome ◽  
Sturge Weber Syndrome ◽  
Neurocutaneous Syndromes

Sturge-Weber syndrome (SWS) is a sporadic disorder and is frequent among the neurocutaneous syndromes specifically with vascular predominance. This syndrome consists of constellation of clinical features like facial nevus, seizures, hemiparesis, intracranial calcifications, and mental retardation. It is characterized by focal port-wine stain, ocular abnormalities (glaucoma), and choroidal hemangioma and leptomeningeal angioma most often involving occipital and parietal lobes. The present paper reports three cases of SWS with oral manifestations and periodontal management, which included thorough scaling and root planing followed by gingivectomy with scalpel and laser in cases 1 and 3 consecutively to treat the gingival enlargement. However, the treatment in case 2 was deferred as the patient was not a candidate for periodontal surgery.

THE CHROMOSOMAL CONSTITUTION OF THE STURGE-WEBER SYNDROME

The Lancet ◽  
1961 ◽  
Vol 277 (7176) ◽  
pp. 558-559 ◽  
Author(s):  
M.D. Hayward ◽  
B.D. Bower ◽  
K.-H. Gustavson ◽  
O. Höök ◽  
Bertil Hall
Keyword(s):  
Chromosomal Constitution ◽  
Weber Syndrome ◽  
Sturge Weber Syndrome
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