Double trouble: Bilateral cerebral involvement in Sturge-Weber syndrome

SA Journal of Radiology

 
 
Field Value
 
Title Double trouble: Bilateral cerebral involvement in Sturge-Weber syndrome
 
Creator Adroos, Narosha Smal, Janet Suleman, Farhana E.
 
Subject — —
Description Sturge-Weber syndrome, also known as encephalotrigeminal angiomatosis or meningofacial angiomatosis, is characterised in its classical form by a congenital, usually unilateral, ‘portwine stain’ (capillary naevus) on the face, convulsions, typical intracranial calcification and some degree of mental retardation and hemiparesis. The clinical correlation of intractable seizures with the presence of bilateral intracranial disease has management and prognostic implications, thus making the presence of bilateral disease an important factor to all those involved in the management of the child with Sturge-Weber syndrome.
 
Publisher AOSIS
 
Contributor not applicable
Date 2015-08-14
 
Type info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion — case series
Format text/html application/octet-stream text/xml application/pdf
Identifier 10.4102/sajr.v19i1.760
 
Source South African Journal of Radiology; Vol 19, No 1 (2015); 4 pages 2078-6778 1027-202X
 
Language eng
 
Relation
The following web links (URLs) may trigger a file download or direct you to an alternative webpage to gain access to a publication file format of the published article:

https://sajr.org.za/index.php/sajr/article/view/760/999 https://sajr.org.za/index.php/sajr/article/view/760/1001 https://sajr.org.za/index.php/sajr/article/view/760/1002 https://sajr.org.za/index.php/sajr/article/view/760/985
 
Coverage South Africa historical not applicable
Rights Copyright (c) 2015 Narosha Adroos, Janet Smal, Farhana E. Suleman https://creativecommons.org/licenses/by/4.0
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