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性早熟:生长与遗传学

Precocious puberty: growth and genetics.

作者信息

Phillip Moshe, Lazar Liora

机构信息

Institute for Endocrinology and Diabetes, National Center for Childhood Diabetes, Schneider Children's Medical Center of Israel, Petah-Tiqva, Israel.

出版信息

Horm Res. 2005;64 Suppl 2:56-61. doi: 10.1159/000087760.

Abstract

The precise neuroendocrine mechanisms underlying activation of hypothalamic-pituitary-gonadal (HPG) axis maturation are elusive. The wide age range of pubertal onset among normal individuals throughout the world may suggest that both genetic and environmental factors modulate the timing of puberty. Early activation of the HPG axis, termed central precocious puberty (CPP), causes psychosocial difficulties and may lead to compromised final height, especially if medical intervention is delayed. Although CPP is considered to be idiopathic in the majority of patients, we have recently reported a 27.5% prevalence of familial cases among 147 patients with idiopathic CPP. Segregation analysis of this cohort suggested an autosomal dominant transmission with incomplete sex-dependent penetrance. Allelic variants of candidate genes that regulate the timing of puberty may cause familial CPP. Detection of these genes will provide a tool for identification of children at risk of developing CPP, enabling early intervention with the aim of preventing its distressing outcomes.

摘要

下丘脑-垂体-性腺(HPG)轴成熟激活背后的确切神经内分泌机制尚不清楚。世界各地正常个体青春期开始的年龄范围很广,这可能表明遗传和环境因素都对青春期的时间有调节作用。HPG轴的过早激活,即中枢性性早熟(CPP),会导致心理社会问题,并可能导致最终身高受损,尤其是在医疗干预延迟的情况下。虽然大多数CPP患者被认为是特发性的,但我们最近报告称,在147例特发性CPP患者中,家族性病例的患病率为27.5%。对该队列的分离分析表明,其遗传方式为常染色体显性遗传,且存在不完全的性别依赖性外显率。调节青春期时间的候选基因的等位基因变异可能导致家族性CPP。检测这些基因将为识别有患CPP风险的儿童提供一种工具,从而能够进行早期干预,以防止出现令人苦恼的后果。

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