Key result
Primary periodic paralyses are hereditary disorders caused by mutations in genes encoding skeletal muscle channel proteins, leading to episodic muscle weakness and paralysis.
Design
Review
Authors
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Supports arrhythmia vigilance in channelopathies; leaves open prospective trials on genotype-guided management.
Primary periodic paralyses are a group of hereditary disorders caused by mutations in skeletal muscle ion channels, leading to episodic muscle weakness and, in some cases, cardiac arrhythmias.
Farooque et al. (2020) conducted a review in Primary periodic paralyses. Primary periodic paralyses are hereditary disorders caused by mutations in genes encoding skeletal muscle channel proteins, leading to episodic muscle weakness and paralysis.
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