familial dysalbuminemic hyperthyroxinaemia
familial dysalbuminemic hyperthyroxinaemiaAn 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 .
FDH is caused by a mutation of ALB on chromosome 4q13.3.
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