paralysis periodica paramyotonica caused by scn4a arg1448cys mutation

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ID: 172533
2006
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Ranked #220 of 246 articles by views in Bioorganic & medicinal chemistry letters

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Abstract
Paralysis periodica paramyotonica is an overlapping disease that shares the features of paramyotonia characteristic of paramyotonia congenita (PC) and periodic paralysis characteristic of hyperkalemic periodic paralysis. We report the case of a 23-year-old man with paralysis periodica paramyotonica. His father and a younger brother also exhibited a similar phenotype. A SCN4A Arg1448Cys mutation was detected in this family. The affected family members exhibited marked shifts in compound muscle action potential amplitudes on exercise test, and muscle weakness could be induced by potassium loading and cold exposure. This case demonstrates that SCN4A Arg1448Cys can produce paralysis periodica paramyotonica. Other genetic or environmental factors may modulate the manifestation of SCN4A Arg1448Cys mutation.
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hsu2006journalparalysis Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors ;Wei-Chih Hsu;Yung-Chuan Huang;Chung-Wei Wang;Chia-Hsiang Hsueh;Ling-Ping Lai;Jiann-Horng Yeh
Journal Bioorganic & medicinal chemistry letters
Year 2006
DOI
10.1016/S0929-6646(09)60191-1
URL
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