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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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| Publicado no: | Endocrinol Diabetes Metab Case Rep |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Bioscientifica Ltd
2020
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| Assuntos: | |
| Acesso em linha: | 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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