scholarly journals A case of adult-onset Sturge-Weber syndrome type III without intracranial calcification, presenting with transient homonymous hemianopia

2021 ◽  
Vol 61 (2) ◽  
pp. 132-135
Author(s):  
Yuto Hayashi ◽  
Yuri Sugiura ◽  
Rie Nakatani ◽  
Katsuya Araki ◽  
Masayuki Moriya ◽  
...  
2017 ◽  
Vol 57 (5) ◽  
pp. 214-219 ◽  
Author(s):  
Hidehiro Ishikawa ◽  
Yuichiro Ii ◽  
Atsushi Niwa ◽  
Keita Matsuura ◽  
Masayuki Maeda ◽  
...  

2018 ◽  
Vol 5 (2) ◽  
pp. 103-105
Author(s):  
Hande Gazeteci Tekin ◽  
Sarenur Gökben ◽  
Sanem Yılmaz ◽  
Hasan Tekgül ◽  
Gül Serdaroğlu

2014 ◽  
Vol 82 (1) ◽  
pp. 97-98 ◽  
Author(s):  
Devdeep Mukherjee ◽  
Ritabrata Kundu ◽  
Prabal Chandra Niyogi

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.


2013 ◽  
Vol 53 (5) ◽  
pp. 845-849 ◽  
Author(s):  
Hung Yu Huang ◽  
Kang-Hsu Lin ◽  
Jui-Cheng Chen ◽  
Yi-Ting Hsu

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

Author(s):  
MI Ahmed ◽  
P Jordan ◽  
M Arora ◽  
M Iqbal ◽  
S Bandi ◽  
...  

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