Euthyroid dysprealbuminemic hyperthyroxinemia
ORPHA:597939· ICD-10 E07.8
Definition
A rare genetic endocrine disease characterized by increased affinity of a mutated transthyretin for T4. Total and free T4 may be normal or elevated, but affected individuals are clinically euthyroid.
- Prevalence
- <1 / 1 000 000
- Inheritance
- Autosomal dominant
- Age of onset
- Adult