Suppr超能文献

格雷夫斯病伴家族性甲状腺素结合球蛋白缺乏症。

Graves' disease associated with familial deficiency of thyroxine-binding globulin.

作者信息

Horwitz D L, Refetoff S

出版信息

J Clin Endocrinol Metab. 1977 Feb;44(2):242-7. doi: 10.1210/jcem-44-2-242.

Abstract

Five patients presented with symptoms of Graves' disease and a marked decrease in their thyroxine-binding globulin (TBG) capacity. While thyrotoxic, mean values +/- SD for the 5 patients were: total thyroxine (TT4) 8.8+/-2.0 mug/100 ml (normal range 4.4-9.3); TBG capacity 6.1+/-1.1 mug T4/100 ml (normal range 16-24); free thyroxine index (FTI) 25.3+/-8.9 (normal range 3.6-9.3); and total triiodo-thyronine (TT3) 244+/-56 ng/100 ml (normal range 80-160). When euthyroid, both TT4 (2.8+/-0.8 mug/100 ml) and TT3 (68+/-12 ng/100 ml) were below the normal range and FTI (5.8+/-0.6) was normal. All patients were male, and family studies revealed decreased TBG capacity in blood relatives consistent with X-chromosome linked inheritance. All examined relatives relatives of the propositi, whether hemizygous or heterozygous, were euthyroid. Over the same period of time 7 additional patients (excluding family members of propositi) were found to be euthyroid but had decreased TBG capacity. The occurrence of thyrotoxicosis in 5 out of 12 patients with inherited TBG deficiency suggests an association rather than a coincidental finding, although initial tests were performed because of suspected thyroid dysfunction. The incidence of thyrotoxicosis in patients with inherited TBG deficiency is also high on the basis of the reported prevalence of the latter genetic abnormality. This study stresses the importance of determining TT3 and FTI on patients who are clinically thyrotoxic but have normal TT4.

摘要

5例患者出现格雷夫斯病症状,其甲状腺素结合球蛋白(TBG)能力显著降低。在甲状腺毒症期,这5例患者的均值±标准差为:总甲状腺素(TT4)8.8±2.0μg/100ml(正常范围4.4 - 9.3);TBG能力6.1±1.1μg T4/100ml(正常范围16 - 24);游离甲状腺素指数(FTI)25.3±8.9(正常范围3.6 - 9.3);总三碘甲状腺原氨酸(TT3)244±56ng/100ml(正常范围80 - 160)。在甲状腺功能正常期,TT4(2.8±0.8μg/100ml)和TT3(68±12ng/100ml)均低于正常范围,而FTI(5.8±0.6)正常。所有患者均为男性,家族研究显示血缘亲属的TBG能力降低,符合X染色体连锁遗传。所有被检查的先证者亲属,无论半合子还是杂合子,甲状腺功能均正常。在同一时期,另外7例患者(不包括先证者的家庭成员)被发现甲状腺功能正常,但TBG能力降低。12例遗传性TBG缺乏患者中有5例发生甲状腺毒症,这表明两者之间存在关联而非偶然发现,尽管最初的检查是由于怀疑甲状腺功能障碍而进行的。根据报道的后一种基因异常的患病率,遗传性TBG缺乏患者中甲状腺毒症的发生率也很高。本研究强调了对临床甲状腺毒症但TT4正常的患者测定TT3和FTI的重要性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验