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甲状腺素结合球蛋白(TBG)缺乏症是一种X性联显性遗传性疾病。本症首先由Tanaka和Sta-rr于1959年报告,近来通过克订病筛选检查发现本症并不少见。Horwitz和Refetoff在20,000例甲
Thyroxine-binding globulin (TBG) deficiency is a X-linked dominant genetic disorder. The disease was first reported by Tanaka and Sta-rr in 1959, and it was not uncommon to find this disease recently confirmed by a screening test. Horwitz and Refetoff in 20,000 cases