MON-483 Familial Dysalbuminemic Hyperthyroxinemia with False Hypercortisolemia

Background: Familial dysalbuminemic hyperthyroxinemia (FDH) is an autosomal dominant disease characterized by hyperthyroxinemia without symptoms of thyrotoxicosis, due to a high affinity of mutant albumin for thyroxine. No report has described cortisol-albumin binding in FDH patient, and here we pre...

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Detalles Bibliográficos
Autores principales: Chiba, Koki, Kameda, Hiraku, Nomoto, Hiroshi, Cho, Kyu Yong, Nakamura, Akinobu, Jin, Shigeki, Matoba, Kotaro, Miyoshi, Hideaki, Atsumi, Tatsuya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Thyroid
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7208649/
http://dx.doi.org/10.1210/jendso/bvaa046.409

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7208649/
http://dx.doi.org/10.1210/jendso/bvaa046.409

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