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Article

Hyperthyroxinemia and Hypercortisolemia due to Familial Dysalbuminemia.

Thyroid : official journal of the American Thyroid Association - 1 Nov 2020

Moran Carla, Seger Christoph, Taylor Kevin, Oddy Susan, Burling Keith, Rajanayagam Odelia, Fairall Louise, McGowan Anne, Lyons Greta, Halsall David, Gurnell Mark, Schwabe John, Chatterjee Krishna, Strey Christopher

Abstract excerpt

A 23-year-old man and his grandmother with hyperthyroxinemia and hypercortisolemia were heterozygous for an ALB mutation (p. Arg218Pro), known to cause familial dysalbuminemic hyperthyroxinemia (FDH). However, serum-free cortisol levels in these individuals were normal and total cortisol concentrations fell markedly after depletion of albumin from their serum. We conclude that binding of steroid as well as...

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Identifiers

PMID: 32669045
DOI: 10.1089/thy.2020.0315
PMCID: PMC7692891

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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