scholarly journals Thyrotoxic periodic paralysis in an adolescent male: A case report and literature review

2020 ◽  
Author(s):  
Luke He ◽  
Veronica Lawrence ◽  
Wayne V. Moore ◽  
Yun Yan
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Periodic Paralysis ◽  
Adolescent Male ◽  
Thyrotoxic Periodic Paralysis

scholarly journals Thyrotoxic Periodic Paralysis: A Case Report and Literature Review

2009 ◽  
Vol 7 (3) ◽  
pp. 96-98 ◽  
Author(s):  
M. J. Barahona ◽  
I. Vinagre ◽  
L. Sojo ◽  
J. M. Cubero ◽  
A. Perez
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Periodic Paralysis ◽  
Thyrotoxic Periodic Paralysis

Ventricular tachycardia secondary to thyrotoxic periodic paralysis: A case report

2021 ◽  
Author(s):  
Juan Duarte Torres ◽  
Alexander Marschall ◽  
Cristina Fraile Sanz ◽  
Belen Biscotti Rodíl ◽  
Hugo del Castillo Carnevali ◽  
...  
Keyword(s):  
Ventricular Tachycardia ◽  
Case Report ◽  
Periodic Paralysis ◽  
Thyrotoxic Periodic Paralysis

Thyrotoxic periodic paralysis presenting in an adult male from Cambodia: a case report

2021 ◽  
Author(s):  
Bensmaine Faïza ◽  
Barrande Gaelle ◽  
Desaint Paul ◽  
Jardin Alexis ◽  
Plantefeve Gaetan ◽  
...  
Keyword(s):  
Case Report ◽  
Adult Male ◽  
Periodic Paralysis ◽  
Thyrotoxic Periodic Paralysis

scholarly journals Hyperkalemic Periodic Paralysis: Case Report with a SCNA4 Gene Mutation and Literature Review

2020 ◽  
Vol 2020 ◽  
pp. 1-4
Author(s):  
Manuela Quiroga-Carrillo ◽  
Cristian Correa-Arrieta ◽  
Fernando Ortiz-Corredor ◽  
Fernando Suarez-Obando
Keyword(s):  
Physical Activity ◽  
Case Report ◽  
Literature Review ◽  
Point Mutation ◽  
Gene Mutation ◽  
Musculoskeletal Disorder ◽  
Autosomal Dominant ◽  
Point Mutations ◽  
Periodic Paralysis ◽  
Hyperkalemic Periodic Paralysis

Hyperkalemic periodic paralysis is a rare musculoskeletal disorder characterized by episodic muscle weakness associated with hyperkalemia. It is a channelopathy associated with point mutations in the SCNA4 gene, with an autosomal dominant pattern of inheritance. We report the case of a 39-year-old patient with a picture with onset at six years of age, consisting of episodes of weakness caused by physical activity and intercurrent infectious processes, in whom a point mutation was found in the SCNA4 gene, not previously reported in the literature.

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