Hyperthyroxinemia and Hypercortisolemia due to Familial Dysalbuminemia

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 concentrati...

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Dades bibliogràfiques
Publicat a:Thyroid
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: Mary Ann Liebert, Inc., publishers 2020
Matèries:
Brief Reports
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7692891/
https://ncbi.nlm.nih.gov/pubmed/32669045
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/thy.2020.0315
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