Abstract:We report a case with hereditary hypokalemic paralysis type 2 in whom thyrotoxicosis aggravated his attacks of paralysis. He experienced paralytic attacks several times a year from 24 years of age and was clinically diagnosed with hypokalemic periodic paralysis. At 49 years of age, a laboratory examination showed normal thyroid function. At 57 years of age, transient thyrotoxicosis was accompanied with an increase of the frequency and severity of attacks. Gene analysis revealed a missense mutation (c.2015G>A, … Show more
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