Literature DB >> 8767512

Diagnosis of thyroid hormone transport protein anomalies: an overview.

W Langsteger1.   

Abstract

Inherited or acquired variations in the serum concentrations of TBG, TTR or albumin are rather common. Clinical studies have shown that most patients with transport protein variations were referred for thyroid testing because of incidentally detected "unusual" thyroid function tests. Although, usually no palpable thyroid abnormalities were found, the interpretation of these unexpected thyroid function tests resulted very often in inappropriate treatment with surgery, 131-iodine, antithyroid drugs as well as T4-replacement therapy. The clinical impact in the interpretation and diagnosis of thyroid hormone transport protein variations is to prevent these patients of unnecessary and sometimes also contraindicated treatment. If changes in thyroid hormone transport proteins in individuals with thyroid disorders or in individuals with the coexistence of two inherited defects are seen, difficulties in the interpretation of thyroid function tests will still occur.

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Year:  1996        PMID: 8767512

Source DB:  PubMed          Journal:  Acta Med Austriaca        ISSN: 0303-8173


  2 in total

1.  An association study between the transthyretin (TTR) gene and mental retardation.

Authors:  Jun Li; Jian-Jun Gao; Fu-Chang Zhang; Qing-He Xing; Fang-Li Dang; Xiao-Cai Gao; Shi-Wei Duan; Zi-Jian Zheng; Xue-Qing Qian; Wei Qin; Xing-Wang Li; Yan-Feng Han; Jing Li; Guo-Yin Feng; D St Clair; Lin He
Journal:  Eur Arch Psychiatry Clin Neurosci       Date:  2005-12-19       Impact factor: 5.270

2.  Identification of a novel mutation in thyroxine-binding globulin (TBG) gene associated with TBG-deficiency and its effect on the thyroid function.

Authors:  S Gawandi; K Jothivel; S Kulkarni
Journal:  J Endocrinol Invest       Date:  2021-11-10       Impact factor: 4.256

  2 in total

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