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familial dysalbuminemic hyperthyroxinemia

Etiology: - increase affinity of albumin for thyroxine (T4) Epidemiology: - most common cause of inherited euthyroid hyperthyroxinemia in Caucasian population Genetics: - associated with defects in albumin Clinical manifestations: - persons are euthyroid Laboratory: - serum thyroxine is increased - free T4 is normal or increased - serum TSH should be low to normal

General

euthyroid hyperthyroxinemia inborn error of metabolism

Database Correlations

OMIM 103600 MORBIDMAP 103600

References

OMIM :accession 103600