First Report of Familial Dysalbuminemic Hyperthyroxinemia With an ALB Variant

Familial dysalbuminemic hyperthyroxinemia (FDH) is an inherited disease characterized by increased circulating total thyroxine (T4) levels and normal physiological thyroid function. Heterozygous albumin gene (ALB) variants have been reported to be the underlying cause of FDH. To our knowledge, there...

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Detalles Bibliográficos
Autores principales: Cho, Yoon Young, Song, Ju-Sun, Park, Hyung-Doo, Kim, Young Nam, Kim, Hye-In, Kim, Tae Hyuk, Chung, Jae Hoon, Ki, Chang-Seok, Kim, Sun Wook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Laboratory Medicine 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5107620/
https://www.ncbi.nlm.nih.gov/pubmed/27834068
http://dx.doi.org/10.3343/alm.2017.37.1.63

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5107620/
https://www.ncbi.nlm.nih.gov/pubmed/27834068
http://dx.doi.org/10.3343/alm.2017.37.1.63

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