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中枢性甲状腺功能减退症的遗传学方面

Genetic aspects of central hypothyroidism.

作者信息

Collu R

机构信息

Division of Endocrinology, University of Ancona, Torrette Hospital, Italy.

出版信息

J Endocrinol Invest. 2000 Feb;23(2):125-34. doi: 10.1007/BF03343692.

Abstract

Central hypothyroidism, characterized by insufficient TSH secretion in the presence of low levels of thyroid hormones, is a rare disorder. It has recently been found that, although mainly due to tumors or infiltrative diseases of the hypothalamo-pituitary area or to pituitary atrophy, central hypothyroidism may be caused by inactivating mutations in several of the genes that code for the various proteins involved in the regulation of the hypothalamo-pituitary-thyroid axis (HPTA). These experiments of nature allow us to better understand the pathophysiology but also the normal physiology of the HPTA. This review will analyze reports of mutations that affect the HPTA and result in either isolated central hypothyroidism or in the syndrome of combined pituitary hormone deficiency (CPHD). Mutations have been identified in the genes for the TRH receptor, the transcription factors Pit-1 and PROP1, and the TSH beta-subunit.

摘要

中枢性甲状腺功能减退症是一种罕见的疾病,其特征是在甲状腺激素水平较低的情况下促甲状腺激素(TSH)分泌不足。最近发现,虽然中枢性甲状腺功能减退症主要由下丘脑 - 垂体区域的肿瘤或浸润性疾病或垂体萎缩引起,但也可能由编码参与下丘脑 - 垂体 - 甲状腺轴(HPTA)调节的各种蛋白质的多个基因的失活突变引起。这些自然发生的实例使我们能够更好地理解HPTA的病理生理学以及正常生理学。本综述将分析影响HPTA并导致孤立性中枢性甲状腺功能减退症或联合垂体激素缺乏症(CPHD)综合征的突变报告。已在促甲状腺激素释放激素(TRH)受体、转录因子Pit-1和PROP1以及TSHβ亚基的基因中鉴定出突变。

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