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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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:J Endocr Soc
Egile Nagusiak: Chiba, Koki, Kameda, Hiraku, Nomoto, Hiroshi, Cho, Kyu Yong, Nakamura, Akinobu, Jin, Shigeki, Matoba, Kotaro, Miyoshi, Hideaki, Atsumi, Tatsuya
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Oxford University Press 2020
Gaiak:
Thyroid
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC7208649/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvaa046.409
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