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单基因性生长激素缺乏症的经验教训。

Lessons from monogenic causes of growth hormone deficiency.

作者信息

Brue Thierry, Saveanu Alexandru, Jullien Nicolas, Fauquier Teddy, Castinetti Frédéric, Enjalbert Alain, Barlier Anne, Reynaud Rachel

机构信息

Unité mixte de recherche 7286, centre de recherche en neurobiologie et neurophysiologie de Marseille (CRN2M), Centre national de la recherche scientifique, faculté de médecine de Marseille, Aix-Marseille université, 13284 Marseille, France; Department of endocrinology, hôpital de la Conception, 13005 Marseille, France; Centre de référence des maladies rares de l'hypophyse, hôpital de la Conception, 13005 Marseille, France.

Unité mixte de recherche 7286, centre de recherche en neurobiologie et neurophysiologie de Marseille (CRN2M), Centre national de la recherche scientifique, faculté de médecine de Marseille, Aix-Marseille université, 13284 Marseille, France; Department of endocrinology, hôpital de la Conception, 13005 Marseille, France; Centre de référence des maladies rares de l'hypophyse, hôpital de la Conception, 13005 Marseille, France; Laboratory of biochemistry and molecular biology, hôpital de la Conception, 13005 Marseille, France.

出版信息

Ann Endocrinol (Paris). 2017 Jun;78(2):77-79. doi: 10.1016/j.ando.2017.04.001. Epub 2017 May 5.

Abstract

Through the multicentric international GENHYPOPIT network, 10 transcription factor genes involved in pituitary development have been screened in more than 1200 patients with constitutional hypopituitarism over the past two decades. The present report summarizes the main lessons learned from this phenotype-based genetic screening: (1) genetically determined hypopituitarism does not necessarily present during childhood; (2) constitutional hypopituitarism may be characterized by a pure endocrine phenotype or by various combinations of endocrine deficits and visceral malformations; (3) syndromic hypopituitarism may also be observed in patients with POU1F1 or PROP1 mutations; (4) in cases of idiopathic hypopituitarism, extensive genetic screening identifies gene alterations in a minority of patients; (5) functional studies are imperfect in determining the involvement of an allelic variant in a specific pituitary phenotype.

摘要

在过去二十年中,通过多中心国际GENHYPOPIT网络,对1200多名先天性垂体功能减退患者筛查了10个参与垂体发育的转录因子基因。本报告总结了基于该表型的基因筛查所获得的主要经验教训:(1)基因决定的垂体功能减退不一定在儿童期出现;(2)先天性垂体功能减退可能表现为单纯内分泌表型,或内分泌缺陷与内脏畸形的各种组合;(3)POU1F1或PROP1突变患者中也可观察到综合征性垂体功能减退;(4)在特发性垂体功能减退病例中,广泛的基因筛查仅在少数患者中发现基因改变;(5)功能研究在确定等位基因变异与特定垂体表型的关联方面并不完善。

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