Familial dysalbuminemic hyperthyroxinemia combined with Graves ’ disease: a rare case report

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 ...

Source: BMC Endocrine Disorders - October 18, 2023 Category: Endocrinology Authors: Yuanmeng Li, Yue Chi, Xiaofeng Chai, He Liu, Naishi Li and Xiaolan Lian Tags: Case Report Source Type: research