Literature DB >> 34617615

Genetics of pubertal delay.

Tansit Saengkaew1,2, Sasha R Howard1.   

Abstract

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.
© 2021 The Authors. Clinical Endocrinology published by John Wiley & Sons Ltd.

Entities:  

Keywords:  delayed puberty; hypogonadotropic hypogonadism; puberty

Mesh:

Year:  2021        PMID: 34617615      PMCID: PMC9543006          DOI: 10.1111/cen.14606

Source DB:  PubMed          Journal:  Clin Endocrinol (Oxf)        ISSN: 0300-0664            Impact factor:   3.523


  110 in total

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Authors:  Ines L Sedlmeyer; Joel N Hirschhorn; Mark R Palmert
Journal:  J Clin Endocrinol Metab       Date:  2002-12       Impact factor: 5.958

2.  A family with hypogonadotropic hypogonadism and mutations in the gonadotropin-releasing hormone receptor.

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3.  LGR4 deficiency results in delayed puberty through impaired Wnt/β-catenin signaling.

Authors:  Alessandra Mancini; Sasha R Howard; Federica Marelli; Claudia P Cabrera; Michael R Barnes; Michael Je Sternberg; Morgane Leprovots; Irene Hadjidemetriou; Elena Monti; Alessia David; Karoliina Wehkalampi; Roberto Oleari; Antonella Lettieri; Valeria Vezzoli; Gilbert Vassart; Anna Cariboni; Marco Bonomi; Marie Isabelle Garcia; Leonardo Guasti; Leo Dunkel
Journal:  JCI Insight       Date:  2020-06-04

4.  Heparan sulfate 6-O-sulfotransferase 1, a gene involved in extracellular sugar modifications, is mutated in patients with idiopathic hypogonadotrophic hypogonadism.

Authors:  Janne Tornberg; Gerasimos P Sykiotis; Kimberly Keefe; Lacey Plummer; Xuan Hoang; Janet E Hall; Richard Quinton; Stephanie B Seminara; Virginia Hughes; Guy Van Vliet; Stan Van Uum; William F Crowley; Hiroko Habuchi; Koji Kimata; Nelly Pitteloud; Hannes E Bülow
Journal:  Proc Natl Acad Sci U S A       Date:  2011-06-23       Impact factor: 11.205

Review 5.  Uncertainty in childhood illness: a synthesis of the parent and child literature.

Authors:  J L Stewart; M H Mishel
Journal:  Sch Inq Nurs Pract       Date:  2000

6.  Reversal of idiopathic hypogonadotropic hypogonadism.

Authors:  Taneli Raivio; John Falardeau; Andrew Dwyer; Richard Quinton; Frances J Hayes; Virginia A Hughes; Lindsay W Cole; Simon H Pearce; Hang Lee; Paul Boepple; William F Crowley; Nelly Pitteloud
Journal:  N Engl J Med       Date:  2007-08-30       Impact factor: 91.245

Review 7.  The role of the FTO (Fat Mass and Obesity Related) locus in regulating body size and composition.

Authors:  Giles S H Yeo
Journal:  Mol Cell Endocrinol       Date:  2014-09-16       Impact factor: 4.102

8.  Dax1 antagonizes Sry action in mammalian sex determination.

Authors:  A Swain; V Narvaez; P Burgoyne; G Camerino; R Lovell-Badge
Journal:  Nature       Date:  1998-02-19       Impact factor: 49.962

Review 9.  Recent advances in understanding primary ovarian insufficiency.

Authors:  Victoria Wesevich; Amanada N Kellen; Lubna Pal
Journal:  F1000Res       Date:  2020-09-07

10.  Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism.

Authors:  F Muscatelli; T M Strom; A P Walker; E Zanaria; D Récan; A Meindl; B Bardoni; S Guioli; G Zehetner; W Rabl
Journal:  Nature       Date:  1994-12-15       Impact factor: 49.962

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  1 in total

Review 1.  Genetics of pubertal delay.

Authors:  Tansit Saengkaew; Sasha R Howard
Journal:  Clin Endocrinol (Oxf)       Date:  2021-10-13       Impact factor: 3.523

  1 in total

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