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Hyperthyroxinemia and Hypercortisolemia due to Familial Dysalbuminemia
A 23-year-old man and his grandmother with hyperthyroxinemia and hypercortisolemia were heterozygous for an ALB mutation (p. Arg218Pro), known to cause familial dysalbuminemic hyperthyroxinemia (FDH). However, serum-free cortisol levels in these individuals were normal and total cortisol concentrati...
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| Publicat a: | Thyroid |
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| Autors principals: | , , , , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Mary Ann Liebert, Inc., publishers
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7692891/ https://ncbi.nlm.nih.gov/pubmed/32669045 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/thy.2020.0315 |
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