Familial Dysalbuminemic Hyperthyroxinemia in a Japanese Man Caused by a Point Albumin Gene Mutation (R218P)

Familial dysalbuminemic hyperthyroxinemia (FDH) is a familial autosomal dominant disease caused by mutation in the albumin gene that produces a condition of euthyroid hyperthyroxinemia. In patients with FDH, serum-free thyroxine (FT4) and free triiodothyronine (FT3) concentrations as measured by sev...

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Bibliographic Details
Published in:Jpn Clin Med
Main Authors: Osaki, Yoshinori, Hayashi, Yoshitaka, Nakagawa, Yoshinori, Yoshida, Katsumi, Ozaki, Hiroshi, Fukazawa, Hiroshi
Format: Artigo
Language:Inglês
Published: Libertas Academica 2016
Subjects:
Case Report
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC4821441/
https://ncbi.nlm.nih.gov/pubmed/27081329
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4137/JCM.S38990
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