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Article

[Recent progress on the searchs of pathogenesis of thyrotoxic periodic paralysis].

Nihon rinsho. Japanese journal of clinical medicine - 1 Dec 2006

Shishiba Yoshiaki

Abstract excerpt

In Japan, more than 60% of hypokalemic periodic paralysis is thyrotoxic instead of familial type frequently experienced in Caucasian countries. The pathogenesis of familial hypokalemic periodic paralysis (FHPP) has been elucidated to be due to the mutation of one of the genes in either Ca(CACN1AS), Na(SCN4A) or K channel(KCNE3). Clinical features of thyrotoxic periodic paralysis (TPP) is very similar to that of...

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PMID: 17154102

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[Familial hypokalemic periodic paralysis].Semantic proximity Read ↗

[A novel mutation of SCN4A gene causes hypokalemic periodic paralysis in a Chinese family].Semantic proximity Read ↗

[R1239H mutation of CACNA1S gene in a Chinese family with hypokalaemic periodic paralysis].Semantic proximity Read ↗

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Manifestation, Management and Molecular Analysis of Candidate Genes in Two Rare Cases of Thyrotoxic Hypokalemic Periodic ParalysisSemantic proximity Read ↗

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