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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Bibliografiske detaljer
Udgivet i:J Endocr Soc
Main Authors: Nagano, Hidekazu, Hashimoto, Naoko, Fujimoto, Masanori, Nakayama, Akitoshi, Miyabayashi, Yui, Yue, Yao, Yue, Gao, Higuchi, Seiichiro, Tanaka, Tomoaki
Format: Artigo
Sprog:Inglês
Udgivet: Endocrine Society 2019
Fag:
Thyroid
Online adgang: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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