Familial dysalbuminaemic hyperthyroxinaemia interferes with current free thyroid hormone immunoassay methods

OBJECTIVE: Familial dysalbuminaemic hyperthyroxinaemia (FDH), most commonly due to an Arginine to Histidine mutation at residue 218 (R218H) in the albumin gene, causes artefactual elevation of free thyroid hormones in euthyroid individuals. We have evaluated the susceptibility of most current free t...

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Detalles Bibliográficos
Autores principales: Khoo, Serena, Lyons, Greta, McGowan, Anne, Gurnell, Mark, Oddy, Susan, Visser, W Edward, van den Berg, Sjoerd, Halsall, David, Taylor, Kevin, Chatterjee, Krishna, Moran, Carla
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2020
Materias:
Clinical Study
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7222281/
https://www.ncbi.nlm.nih.gov/pubmed/32213658
http://dx.doi.org/10.1530/EJE-19-1021

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7222281/
https://www.ncbi.nlm.nih.gov/pubmed/32213658
http://dx.doi.org/10.1530/EJE-19-1021

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