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Article

Genotype and phenotype analysis of patients with sporadic periodic paralysis.

The American journal of the medical sciences - 1 Apr 2012

Sung Chih-Chien, Cheng Chih-Jen, Lo Yi-Fen, Lin Mei-Shan, Yang Sung-Sen, Hsu Yu-Chuan, Lin Shih-Hua

Abstract excerpt

INTRODUCTION: Sporadic periodic paralysis (SPP), the second leading cause of hypokalemic periodic paralysis (HPP) in Asia, has a presentation similar to that of familial periodic paralysis (FPP) and is caused by gene mutations in the calcium (Ca(2+)) (CACNA1S) and sodium (Na(+)) (SCN4A) channels of skeletal muscle. The authors determined whether SPP shares similar genotype and phenotype with FPP. METHODS: Sixty...

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PMID: 21841462
DOI: 10.1097/MAJ.0b013e31822b430c

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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