Effect of Albumin Polymorphism on Thyroid Hormones: A Case Report and Literature Review

Familial dysalbuminemic hyperthyroxinemia (FDH) is the most common cause of the inherited increase of serum thyroxine in Caucasians. This disorder occurs due to a missense mutation in the human serum albumin, resulting in an increased affinity of thyroxine to the binding sites on the human serum alb...

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Detalles Bibliográficos
Autores principales: Mahendhar, Rupak, Shahbaz, Amir, Riaz, Maria, Aninyei, Michael, Reich, David M, Sachmechi, Issac
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2018
Materias:
Endocrinology/Diabetes/Metabolism
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6126704/
https://www.ncbi.nlm.nih.gov/pubmed/30197844
http://dx.doi.org/10.7759/cureus.2903

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6126704/
https://www.ncbi.nlm.nih.gov/pubmed/30197844
http://dx.doi.org/10.7759/cureus.2903

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