甲状腺素结合球蛋白的遗传性异常，无明显甲状腺素结合活性，血清中变性甲状腺素结合球蛋白水平升高。 - Suppr

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超能文献

Inherited abnormality of thyroxine-binding globulin with no demonstrable thyroxine-binding activity and high serum levels of denatured thyroxine-binding globulin.

作者信息

Murata Y, Takamatsu J, Refetoff S

出版信息

N Engl J Med. 1986 Mar 13;314(11):694-9. doi: 10.1056/NEJM198603133141107.

DOI:10.1056/NEJM198603133141107

PMID:3081807

Abstract

摘要

相似文献

Inherited abnormality of thyroxine-binding globulin with no demonstrable thyroxine-binding activity and high serum levels of denatured thyroxine-binding globulin.甲状腺素结合球蛋白的遗传性异常，无明显甲状腺素结合活性，血清中变性甲状腺素结合球蛋白水平升高。

N Engl J Med. 1986 Mar 13;314(11):694-9. doi: 10.1056/NEJM198603133141107.

[Behavior of the levels of free triiodothyronine, triiodothyronine, free thyroxine, thyroxine, thyrotropin and thyroxine-binding globulin in the serum of children with nephrotic syndrome].[肾病综合征患儿血清中游离三碘甲状腺原氨酸、三碘甲状腺原氨酸、游离甲状腺素、甲状腺素、促甲状腺激素及甲状腺素结合球蛋白水平的变化]

Klin Padiatr. 1985 Sep-Oct;197(5):423-6. doi: 10.1055/s-2008-1034015.

[Behavior of the concentration of triiodothyronine, thyroxine, thyrotropin and thyroxine-binding globulin in the serum of children with nephrotic syndrome].[肾病综合征患儿血清中三碘甲状腺原氨酸、甲状腺素、促甲状腺激素及甲状腺素结合球蛋白浓度的变化]

Klin Padiatr. 1985 Jan-Feb;197(1):35-9. doi: 10.1055/s-2008-1033923.

[A family with hereditary increase in thyroxine-binding globulin].[一个甲状腺素结合球蛋白遗传性增加的家族]

Dtsch Med Wochenschr. 1972 Feb 11;97(6):194-6. doi: 10.1055/s-0028-1107324.

Hereditary abnormalities of thyroxine-binding globulin concentration. A study of 19 kindreds with inherited increase or decrease of thyroxine-binding globulin.甲状腺素结合球蛋白浓度的遗传性异常。对19个家系进行的研究，这些家系中甲状腺素结合球蛋白存在遗传性增加或减少的情况。

Q J Med. 1980;49(195):295-313.

Interpretation of serum tri-iodothyronine levels measured by the sterling technic.采用斯特林技术测定血清三碘甲状腺原氨酸水平的解读

N Engl J Med. 1971 Feb 4;284(5):225-30. doi: 10.1056/NEJM197102042840501.

Abnormal thyroxine and triiodothyronine concentration in the blood due to familial disorders in the thyroxine-binding globulin concentration.由于甲状腺素结合球蛋白浓度的家族性疾病导致血液中甲状腺素和三碘甲状腺原氨酸浓度异常。

Ned Tijdschr Geneeskd. 1974 Jul 20;118(29):1115-21.

Normal response to thyrotrophin releasing hormone (TRH) in familial thyroxine-binding globulin deficiency.家族性甲状腺素结合球蛋白缺乏症患者对促甲状腺激素释放激素（TRH）的正常反应。

Acta Endocrinol (Copenh). 1975 Oct;80(2):279-301.

Concordant decreases of thyroxine and thyroxine binding protein concentrations during sepsis.脓毒症期间甲状腺素和甲状腺素结合蛋白浓度的一致性降低。

Metabolism. 2000 Jun;49(6):753-4. doi: 10.1053/meta.2000.6239.

Hereditary increased thyroxine-binding-globulin capacity.

Mayo Clin Proc. 1972 Oct;47(10):720-4.

引用本文的文献

Partial Thyroid Hormone-Binding Globulin Deficiency: A Case Report and Literature Review.部分甲状腺激素结合球蛋白缺乏症：一例报告及文献综述

Diabetes Metab Syndr Obes. 2023 Jul 26;16:2225-2232. doi: 10.2147/DMSO.S413048. eCollection 2023.

Clinical recognition and evaluation of patients with inherited serum thyroid hormone-binding protein mutations.遗传性血清甲状腺激素结合蛋白突变患者的临床识别和评估。

J Endocrinol Invest. 2020 Jan;43(1):31-41. doi: 10.1007/s40618-019-01084-9. Epub 2019 Jul 27.

TBG deficiency: description of two novel mutations associated with complete TBG deficiency and review of the literature.甲状腺素结合球蛋白缺乏症：与完全性甲状腺素结合球蛋白缺乏相关的两种新突变的描述及文献综述

J Mol Med (Berl). 2006 Oct;84(10):864-71. doi: 10.1007/s00109-006-0078-9. Epub 2006 Sep 1.

Localization of the human thyroxine-binding globulin gene to the long arm of the X chromosome (Xq21-22).人类甲状腺素结合球蛋白基因定位于X染色体长臂（Xq21 - 22）。

Am J Hum Genet. 1987 Sep;41(3):428-35.

Two new inherited defects of the thyroxine-binding globulin (TBG) molecule presenting as partial TBG deficiency.两种新的甲状腺素结合球蛋白（TBG）分子遗传性缺陷，表现为部分TBG缺乏。

J Clin Invest. 1987 Mar;79(3):833-40. doi: 10.1172/JCI112891.

Molecular basis for the properties of the thyroxine-binding globulin-slow variant in American blacks.美国黑人中甲状腺素结合球蛋白慢变体特性的分子基础。

J Endocrinol Invest. 1990 Apr;13(4):343-9. doi: 10.1007/BF03349576.

A new polymorphism of thyroxin-binding globulin in three African groups (Mali) with endemic nodular goitre.在三个患有地方性结节性甲状腺肿的非洲群体（马里）中发现甲状腺素结合球蛋白的一种新的多态性。

Hum Genet. 1992 May;89(2):199-203. doi: 10.1007/BF00217123.

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