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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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| Pubblicato in: | J Endocr Soc |
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| Autori principali: | , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Oxford University Press
2020
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| Soggetti: | |
| Accesso online: | 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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