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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:J Endocr Soc
Egile Nagusiak: Nagano, Hidekazu, Hashimoto, Naoko, Fujimoto, Masanori, Nakayama, Akitoshi, Miyabayashi, Yui, Yue, Yao, Yue, Gao, Higuchi, Seiichiro, Tanaka, Tomoaki
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Endocrine Society 2019
Gaiak:
Thyroid
Sarrera elektronikoa: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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