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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Detalhes bibliográficos
Publicado no:Ann Lab Med
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: The Korean Society for Laboratory Medicine 2017
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5107620/
https://ncbi.nlm.nih.gov/pubmed/27834068
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3343/alm.2017.37.1.63
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