familial dysalbuminemic hyperthyroxinaemia
familial dysalbuminemic hyperthyroxinaemia
An inherited form (OMIM:103600) of euthyroid hyperthyroxinaemia, which is characterised by an increased affinity of albumin for T4. It is the most common cause of inherited euthyroid hyperthyroxinaemia in Caucasians .Molecular pathology
FDH is caused by a mutation of ALB on chromosome 4q13.3.