scholarly journals Isaacs syndrome: the frontier of neurology, psychiatry, immunology and cancer

2020 ◽  
Vol 91 (12) ◽  
pp. 1243-1244
Author(s):  
Susanna B Park ◽  
Rick Thurbon ◽  
Matthew C Kiernan
Keyword(s):  
2020 ◽  
pp. 10.1212/CPJ.0000000000000934
Author(s):  
Andreia Forno ◽  
Alexandra Rodrigues ◽  
Rui Vasconcellos ◽  
Paulo Rego Sousa

Isaacs’ syndrome (IS), also known as acquired neuromyotonia, is a rare neuromuscular disease, manifested by involuntary continuous motor activity.1 Although there are reports in children,2,3 IS is more frequent in adults.1 The clinical presentation can include muscle cramps, fasciculations, myokymia, and pseudomyotonia. Electromyography (EMG) remains the gold standard for diagnosis.1,4 Dysfunction of peripheral nerve voltage-gated potassium channels (VGKC) appears to be related to the development of the disease.1,3,4,5 Paraneoplastic factors also play an important role in IS.5 Anticonvulsants are the first therapeutic option.1,4,5


1995 ◽  
Vol 59 (4) ◽  
pp. 448-448 ◽  
Author(s):  
G Riche ◽  
P Trouillas ◽  
B Bady
Keyword(s):  

1995 ◽  
Vol 58 (3) ◽  
pp. 393-393 ◽  
Author(s):  
B G Van Engelen ◽  
A A Benders ◽  
F J Gabreels ◽  
J H Veerkamp

2015 ◽  
Vol 52 (1) ◽  
pp. 5-12 ◽  
Author(s):  
Aiesha Ahmed ◽  
Zachary Simmons
Keyword(s):  

1996 ◽  
Vol 11 (4) ◽  
pp. 448-449 ◽  
Author(s):  
Paul J. Tuite ◽  
Carlos Navarette ◽  
Vera Bril ◽  
Anthony E. Lang
Keyword(s):  

2016 ◽  
Vol 3 (3) ◽  
pp. 116
Author(s):  
Akam Saeed ◽  
Rebeen Saeed ◽  
Zana Mohammed ◽  
Sarbast Hamid
Keyword(s):  

1996 ◽  
Vol 19 (11) ◽  
pp. 1439-1446 ◽  
Author(s):  
Yoshito Sonoda ◽  
Kimiyoshi Arimura ◽  
Asutsugu Kurono ◽  
Masahito Suehara ◽  
Masaki Kameyama ◽  
...  

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