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促甲状腺激素抵抗综合征

The syndrome of resistance to thyroid stimulating hormone.

作者信息

Refetoff Samuel

机构信息

Department of Medicine, the Committees on Genetics and Molecular Medicine, J. P Kennedy Jr. Mental Retardation Research Center, The University of Chicago, Chicago, Illinois 60637, USA.

出版信息

J Chin Med Assoc. 2003 Aug;66(8):441-52.

Abstract

Resistance to thyroid stimulating hormone (TSH) is a syndrome of reduced sensitivity to a biologically active TSH molecule. Subjects have elevated TSH levels but no goiter. However, thyroid hormone concentration may vary from normal to very high, depending on the severity of the resistance. Individuals with very high TSH, low thyroxine (T4) and hypoplastic thyroid glands can be mistakenly diagnosed as having primary hypothyroidism due a defective development of the thyroid gland. Those with normal or slightly decreased T4 can be misdiagnosed as having central hypothyroidism especially if their serum TSH concentration is only slightly elevated. Mutations in the TSH receptor (TSHr) gene have been reported in fifteen families with homozygous recessive or compound heterozygous inheritance. The mutant TSHrs show reduced or no function due to either altered ligand binding or defect in membrane targeting. Some individuals, heretozygous for a TSHr gene mutation can present mild resistance to TSH manifesting as euthyroidism with slight hyperthyrotropinemia. A larger proportion of families express the phenotype of resistance to TSH in the absence of a TSHr defect. In many the inheritance is dominant and the genetic cause has not been yet determined.

摘要

促甲状腺激素(TSH)抵抗是一种对生物活性TSH分子敏感性降低的综合征。患者TSH水平升高,但无甲状腺肿大。然而,甲状腺激素浓度可能从正常到非常高不等,这取决于抵抗的严重程度。TSH非常高、甲状腺素(T4)低且甲状腺发育不全的个体可能会因甲状腺发育缺陷而被误诊为原发性甲状腺功能减退。T4正常或略有降低的患者可能会被误诊为中枢性甲状腺功能减退,尤其是当他们的血清TSH浓度仅略有升高时。在15个具有纯合隐性或复合杂合遗传的家族中报道了促甲状腺激素受体(TSHr)基因突变。由于配体结合改变或膜靶向缺陷,突变的TSHr显示功能降低或无功能。一些杂合子携带TSHr基因突变的个体可能表现出对TSH的轻度抵抗,表现为甲状腺功能正常伴轻度促甲状腺素血症。在没有TSHr缺陷的情况下,更大比例的家族表现出对TSH抵抗的表型。在许多家族中,遗传方式为显性,遗传原因尚未确定。

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