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Familial dysalbuminemic hyperthyroxinemia confounding management of coexistent autoimmune thyroid disease
SUMMARY: Familial dysalbuminemic hyperthyroxinemia (FDH) is a cause of discordant thyroid function tests (TFTs), due to interference in free T4 assays, caused by the mutant albumin. The coexistence of thyroid disease and FDH can further complicate diagnosis and potentially result in inappropriate ma...
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| Publicat a: | Endocrinol Diabetes Metab Case Rep |
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| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Bioscientifica Ltd
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7077549/ https://ncbi.nlm.nih.gov/pubmed/32101523 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1530/EDM-19-0161 |
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