| 单词 |
familial dysalbuminemic hyperthyroxinaemia |
| 释义 |
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. |
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