MON-612 Familial Dysalbuminemic Hyperthyroxinemia Cases in Five Unrelated Japanese Families and the Influences on Free T4 Measurement

Familial dysalbuminemic hyperthyroxinemia (FDH) is caused by abnormal human serum albumin (HSA) with an increased thyroxine (T4) affinity leading to euthyroid hyperthyroxinemia. In Japanese FDH patients with the HSAR218P mutation, not only one-step but also two-step immunoassays for free T4 (FT4) ca...

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Salvato in:
Dettagli Bibliografici
Pubblicato in:J Endocr Soc
Autori principali: Nagano, Hidekazu, Hashimoto, Naoko, Fujimoto, Masanori, Nakayama, Akitoshi, Miyabayashi, Yui, Yue, Yao, Yue, Gao, Higuchi, Seiichiro, Tanaka, Tomoaki
Natura: Artigo
Lingua:Inglês
Pubblicazione: Endocrine Society 2019
Soggetti:
Thyroid
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6550635/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/js.2019-MON-612
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