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Results 1 - 3 of 3 for Familial periodic paralysis
  1. CACNA1S gene 
    ... J. Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a Chinese family. J Mol Med (Berl). 2005 Mar;83(3):203-8. doi: 10.1007/s00109-005-0638-4. Epub 2005 Feb 22. Citation on PubMed or Free ... F. Hypokalemic Periodic Paralysis. 2002 Apr 30 [updated 2018 Jul 26]. In: ...
    https://medlineplus.gov/genetics/gene/cacna1s - Genetics
  2. SCN4A gene 
    ... books/NBK1338/ Citation on PubMed Weber F. Hyperkalemic Periodic Paralysis. 2003 Jul 18 ... Citation on PubMed
    https://medlineplus.gov/genetics/gene/scn4a - Genetics
  3. KCNJ2 gene 
    ... a disorder characterized by episodes of muscle weakness (periodic paralysis), changes in heart rhythm (arrhythmia), and physical abnormalities ... potassium ions out of these cells, resulting in periodic paralysis and an irregular heart rhythm. It is not ...
    https://medlineplus.gov/genetics/gene/kcnj2 - Genetics