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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Detalles Bibliográficos
Autores principales: Nagano, Hidekazu, Hashimoto, Naoko, Fujimoto, Masanori, Nakayama, Akitoshi, Miyabayashi, Yui, Yue, Yao, Yue, Gao, Higuchi, Seiichiro, Tanaka, Tomoaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2019
Materias:
Thyroid
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6550635/
http://dx.doi.org/10.1210/js.2019-MON-612

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6550635/
http://dx.doi.org/10.1210/js.2019-MON-612

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