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Article

The clinical and genetic heterogeneity analysis of five families with primary periodic paralysis.

Channels (Austin, Tex.) - 1 Dec 2021

Wang Quanquan, Zhao Zhe, Shen Hongrui, Bing Qi, Li Nan, Hu Jing

Abstract excerpt

To explore the clinical and genetic characteristics of five families with primary periodic paralysis (PPP). We reviewed clinical manifestations, laboratory results, electrocardiogram, electromyography, muscle biopsy, and genetic analysis from five families with PPP. Five families with PPP included: hypokalemic periodic paralysis type 1 (HypoPP1, CACNA1S, 1/5), hypokalemic periodic paralysis type 2 (HypoPP2,...

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Source

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Identifiers

PMID: 33345742
DOI: 10.1080/19336950.2020.1857980
PMCID: PMC7757828

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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