Genetics of pubertal delay

被引:8
|
作者
Saengkaew, Tansit [1 ,2 ]
Howard, Sasha R. [1 ]
机构
[1] Queen Mary Univ London, Barts & London Sch Med & Dent, William Harvey Res Inst, Ctr Endocrinol, London, England
[2] Prince Songkla Univ, Fac Med, Dept Paediat, Endocrinol Unit, Hat Yai, Thailand
关键词
delayed puberty; hypogonadotropic hypogonadism; puberty; GONADOTROPIN-RELEASING-HORMONE; CONGENITAL HYPOGONADOTROPIC HYPOGONADISM; OF-FUNCTION MUTATIONS; CONSTITUTIONAL DELAY; KALLMANN-SYNDROME; OLFACTORY SYSTEM; SECULAR TRENDS; RECEPTOR GENE; GROWTH; AGE;
D O I
10.1111/cen.14606
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The timing of pubertal development is strongly influenced by the genetic background, and clinical presentations of delayed puberty are often found within families with clear patterns of inheritance. The discovery of the underlying genetic regulators of such conditions, in recent years through next generation sequencing, has advanced the understanding of the pathogenesis of disorders of pubertal timing and the potential for genetic testing to assist diagnosis for patients with these conditions. This review covers the significant advances in the understanding of the biological mechanisms of delayed puberty that have occurred in the last two decades.
引用
收藏
页码:473 / 482
页数:10
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