Hypokalemic Periodic Paralysis-A Case Report

K Radhika, Prasad Kulkarni, Haripriya, Sandhya R, Dinesh Kumar V

Abstract: It is a rare condition in which patients have severe episodes of muscle weakness concomitant to variations in blood potassium levels. It is an Autosomal dominant Condition. Periodic paralysis are channellopathies caused by mutation in genes encoding ion channels. Hypokalemic periodic paralysis is a diagnosis of Exclusion and recovery of weakness following potassium correction supports the diagnosis. Long term goal of therapy is to avoid attacks, Hence patients should be aware of importance of low carbohydrate diet and consequence of intense exercise.

Keywords: Hypokalemic Periodic Paralysis, HypoKPP, Autosomal Dominant, Acute Onset Weakness

How to Cite?: K Radhika, Prasad Kulkarni, Haripriya, Sandhya R, Dinesh Kumar V, "Hypokalemic Periodic Paralysis-A Case Report", Volume 11 Issue 11, November 2022, International Journal of Science and Research (IJSR), Pages: 999-1001, https://www.ijsr.net/getabstract.php?paperid=MR221113221640, DOI: https://dx.doi.org/10.21275/MR221113221640

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