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Article

Severe exacerbation of Andersen-Tawil syndrome secondary to thyrotoxicosis.

Journal of human genetics - 1 Aug 2014

Díaz-Manera Jordi, Querol Luis, Alejaldre Aída, Rojas-García Ricard, Ramos-Fransi Alba, Gallardo Eduard, Illa Isabel

Abstract excerpt

Thyrotoxic periodic paralysis (TPP) is a rare complication of hyperthyroidism characterized by episodes of weakness. Although TPP has been described in patients all over the world, it is especially frequent in Asiatic patients. Recently, two genomewide association studies have found a susceptibility locus on chromosome 17q24.3 near the KCNJ2 gene, which is responsible for another cause of periodic paralysis, the...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 24849934
DOI: 10.1038/jhg.2014.43

Genes

KCNJ2

Provenance

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Severe exacerbation of Andersen-Tawil syndrome secondary to thyrotoxicosis.PMID 24849934Read ↗

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Genome-wide association study identifies a susceptibility locus for thyrotoxic periodic paralysis at 17q24.3.Semantic proximity Read ↗

Mutations in potassium channel Kir2.6 cause susceptibility to thyrotoxic hypokalemic periodic paralysis.Semantic proximity Read ↗

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Andersen-Tawil syndrome: clinical and molecular aspects.Semantic proximity Read ↗

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