Muscle channelopathies: general investigations
Evidence-based neurology checklist on muscle channelopathies: general investigations: Genetic testing Genetic testing Next generation sequencing (NSG) Blood investigations Electromyogram (EMG) Other muscle investigations Cardiac investigations
Genetic testing
- Genetic testing
- Next generation sequencing (NSG)
Blood investigations
Electromyogram (EMG)
Other muscle investigations
Cardiac investigations
References
- Matthews E, Neuwirth C, Jaffer F, et al. Atypical periodic paralysis and myalgia: A novel RYR1 phenotype. Neurology 2018; 90:e412-e418.
- Matthews E, Palace J, Ramdas S, et al. Care recommendations for the investigation and management of children with skeletal muscle channelopathies. Pediatr Neurol 2023; 145:102-111.
- Matthews E, Holmes S, Fialho D. Skeletal muscle channelopathies: a guide to diagnosis and management. Pract Neurol 2021; 21:196-204.
