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...

Descripción completa

Detalles Bibliográficos
Autores principales: Osaki, Yoshinori, Hayashi, Yoshitaka, Nakagawa, Yoshinori, Yoshida, Katsumi, Ozaki, Hiroshi, Fukazawa, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Libertas Academica 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4821441/
https://www.ncbi.nlm.nih.gov/pubmed/27081329
http://dx.doi.org/10.4137/JCM.S38990

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4821441/
https://www.ncbi.nlm.nih.gov/pubmed/27081329
http://dx.doi.org/10.4137/JCM.S38990

Ejemplares similares