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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2015/04/07 22:57:51」(JST)

Hyperthyroxinemia or hyperthyroxinaemia is a thyroid disease where the serum levels of thyroxine are higher than expected.^[1]

The term is sometimes used to refer to hyperthyroidism, but hyperthyroidism is a more general term.

Types include:

References

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Novel insights into the pleiotropic effects of human serum albumin in health and disease.

Ha CE, Bhagavan NV.SourceDepartment of Native Hawaiian Health, University of Hawaii, Honolulu 96813, USA. Electronic address: chungeun@hawaii.edu.
Biochimica et biophysica acta.Biochim Biophys Acta.2013 Dec;1830(12):5486-93. doi: 10.1016/j.bbagen.2013.04.012. Epub 2013 Apr 17.
BACKGROUND: Human serum albumin is the principal protein in human serum. It participates in regulation of plasma oncotic pressure and transports endogenous and exogenous ligands such as thyroxine, free fatty acids, bilirubin, and various drugs. Therefore, studying its ligand binding mechanism is imp
PMID 23602811

Resistance to thyroid hormone mediated by defective thyroid hormone receptor alpha.

Schoenmakers N, Moran C, Peeters RP, Visser T, Gurnell M, Chatterjee K.SourceInstitute of Metabolic Science, University of Cambridge, UK.
Biochimica et biophysica acta.Biochim Biophys Acta.2013 Jul;1830(7):4004-8. doi: 10.1016/j.bbagen.2013.03.018. Epub 2013 Mar 23.
BACKGROUND: Thyroid hormone acts via receptor subtypes (TRα1, TRβ1, TRβ2) with differing tissue distributions, encoded by distinct genes (THRA, THRB). THRB mutations cause a disorder with central (hypothalamic-pituitary) resistance to thyroid hormone action with markedly elevated thyroid hormone
PMID 23528896

Dumitrescu AM, Refetoff S.SourceDepartment of Medicine, The University of Chicago, Chicago, IL, USA.
Biochimica et biophysica acta.Biochim Biophys Acta.2013 Jul;1830(7):3987-4003. doi: 10.1016/j.bbagen.2012.08.005. Epub 2012 Aug 16.
BACKGROUND: Six known steps are required for the circulating thyroid hormone (TH) to exert its action on target tissues. For three of these steps, human mutations and distinct phenotypes have been identified.SCOPE OF REVIEW: The clinical, laboratory, genetic and molecular characteristics of these th
PMID 22986150