scholarly journals Diagnosis: An atypical case of Sturge-Weber syndrome with bilateral facial hemangioma, bilateral intracranial calcification, and megalocornea

2008 ◽  
Vol 28 (2) ◽  
pp. 150-151 ◽  
Author(s):  
Faruk Incecik M. Ozlem Hergüner ◽  
Kenan Ozcan ◽  
Sakir Altunbasak
2015 ◽  
Vol 19 (1) ◽  
Author(s):  
Narosha Adroos ◽  
Janet Smal ◽  
Farhana E. Suleman

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.


2021 ◽  
Vol 61 (2) ◽  
pp. 132-135
Author(s):  
Yuto Hayashi ◽  
Yuri Sugiura ◽  
Rie Nakatani ◽  
Katsuya Araki ◽  
Masayuki Moriya ◽  
...  

1979 ◽  
Vol 8 (1) ◽  
pp. 39-41 ◽  
Author(s):  
A. Alonso ◽  
D. Taboada ◽  
L. Ceres ◽  
J. Beltran ◽  
R. Olague ◽  
...  

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

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