| familial dysalbuminemic h. |
an autosomal dominant disorder in which an elevation in total serum thyroxine suggests hyperthyroidism, but the patient is euthyroid by clinical evaluation and other tests because an excess of T4-binding serum albumin results in normal free thyroxine concentration and triiodothyronine resin uptake.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| familial dyslipidemic h. |
an inherited syndrome of seriously disordered blood lipid levels and essential hypertension.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| familial fat-induced h. |
persistently elevated blood chylomicrons after ingestion of fat; it is characteristic of disorders with a type I hyperlipoproteinemia phenotype and is sometimes used as a synonym for this phenotype or genetic disorders causing it.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| familial h. |
Wilson's disease.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| familial h. with hyperprebetalipoproteinemia |
see familial h.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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