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遗传性甲状腺素结合球蛋白增多症。一个家族的研究。

Inherited thyroxine-binding globulin excess. Study in a kindred.

作者信息

Frank K, Gärtner R, Raue F, Ziegler R

出版信息

Exp Clin Endocrinol. 1986 Dec;88(2):237-41. doi: 10.1055/s-0029-1210602.

Abstract

A three-generation family with hereditary high thyroxine-binding globulin (TBG) serum levels has been studied. All patients were clinically euthyroid and did not have a goiter. Four females of the eleven members of the kindred had elevated TBG (range: 34-56 micrograms/ml), total thyroxine (T4) and total triiodothyronine (T3) levels, but normal free T4 (fT4) and normal response of thyroid stimulating hormone (TSH) to intravenous application of thyrotropin-releasing hormone (TRH). Microheterogeneity of TBG studied by isoelectric focusing showed a normal pattern. No variations of the four main bands as seen in other causes of TBG excess like liver diseases, estrogen therapy or pregnancy could be measured. The changes in TBG concentration seem to be due to an abnormal gene expression controlling synthesis of TBG.

摘要

对一个遗传性血清甲状腺素结合球蛋白(TBG)水平升高的三代家族进行了研究。所有患者临床甲状腺功能正常,且无甲状腺肿。该家族11名成员中有4名女性的TBG(范围:34 - 56微克/毫升)、总甲状腺素(T4)和总三碘甲状腺原氨酸(T3)水平升高,但游离T4(fT4)正常,且甲状腺刺激激素(TSH)对静脉注射促甲状腺激素释放激素(TRH)的反应正常。通过等电聚焦研究的TBG微异质性显示出正常模式。未检测到如肝病、雌激素治疗或妊娠等其他导致TBG升高原因中所见的四条主要条带的变化。TBG浓度的变化似乎是由于控制TBG合成的基因表达异常所致。

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