Andersen-Tawil syndrome (ATS): clinical features
Evidence-based neurology checklist on andersen-tawil syndrome (ats): clinical features: Pathology It is a potassium channelopathy It is usually hypokalaemic It could be normokalaemic or hyperkalaemic Genetic types Neurological features: weakness Triggers of weakness Neurological features: others…
Pathology
- It is a potassium channelopathy
- It is usually hypokalaemic
- It could be normokalaemic or hyperkalaemic
Genetic types
Neurological features: weakness
Triggers of weakness
Neurological features: others
Skeletal features
Cardiac features
References
- Spillane J, Kullmann DM, Hanna MG. Genetic neurological channelopathies: molecular genetics and clinical phenotypes. JNNP 2016; 87:37-48.
- Meola G, Hanna MG, Fontaine B. Diagnosis and new treatment in muscle channelopathies. JNNP 2009; 80:360-365.
- Rakowicz W, Hanna M. Muscle ion channel diseases. ACNR 2003; 3:14-16.
- Pérez-Riera AR, Barbosa-Barros R, Samesina N, et al. Andersen-Tawil syndrome: a comprehensive review. Cardiol Rev 2021; 29:165-177.
- Oz Tuncer G, Teber S, Kutluk MG, Albayrak P, Deda G. Andersen-Tawil syndrome with early onset myopathy: 2 cases. J Neuromuscul Dis 2017; 4:93-95.
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