Familial dysalbuminemic hyperthyroxinemia combined with Graves’ disease: a rare case report
Abstract Background Familial dysalbuminemic hyperthyroxinemia (FDH) is an autosomal dominant disease characterised by an abnormally increased affinity of albumin for serum thyroxine. Assay interference and differential diagnosis remain challenging for FDH. The condition is more complicated when FDH...
Gespeichert in:
| Hauptverfasser: | , , , , , |
|---|---|
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BMC
2023-10-01
|
| Schriftenreihe: | BMC Endocrine Disorders |
| Schlagworte: | |
| Online-Zugang: | https://doi.org/10.1186/s12902-023-01481-5 |
| Tags: |
Keine Tags, Fügen Sie das erste Tag hinzu!
|