| Literature DB >> 27980311 |
Akira Kurozumi1, Yosuke Okada, Tadashi Arao, Yoshiya Tanaka.
Abstract
Approximately 140 different mutations of thyroid hormone receptor β (TRβ) have been identified in resistance to thyroid hormone (RTH). We report herein a middle-aged man with a negative family history who was diagnosed with RTH based on persistent palpitations. Genetic analysis showed a TRβ mutation causing the substitution of alanine for proline 453 (P453A) in exon 10. Since treatment of RTH is different from that of Graves' disease and thyroid stimulating hormone-producing adenoma (TSHoma), a genetic analysis should be performed even in patients who have a negative family history of RTH and who are free of TSHoma when they present with persistent inappropriate secretion of thyroid stimulating hormone (SITSH).Entities:
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Year: 2016 PMID: 27980311 DOI: 10.7888/juoeh.38.291
Source DB: PubMed Journal: J UOEH ISSN: 0387-821X