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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Publicado en:J Endocr Soc
Main Authors: Nagano, Hidekazu, Hashimoto, Naoko, Fujimoto, Masanori, Nakayama, Akitoshi, Miyabayashi, Yui, Yue, Yao, Yue, Gao, Higuchi, Seiichiro, Tanaka, Tomoaki
Formato: Artigo
Idioma:Inglês
Publicado: Endocrine Society 2019
Assuntos:
Thyroid
Acceso en liña: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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