Literature DB >> 11408757

SHOX in short stature syndromes.

R J Blaschke1, G A Rappold.   

Abstract

Linear growth is a multifactorial trait that is influenced and regulated by a combination of environmental and internal factors. Among the intrinsic determinants of final body height, genetic factors have become more and more prominent, and the list of genes involved in growth-related processes has been extended accordingly. One of the most exciting additions to this list is represented by the discovery of the pseudoautosomal gene SHOX. Originally described as a gene responsible for idiopathic short stature, it has become clear that SHOX mutations can also cause mesomelic short stature and Madelung deformity in Léri-Weill syndrome. In addition, recent studies implicate SHOX haploinsufficiency in a variety of somatic Turner syndrome stigmata. Copyright 2001 S. Karger AG, Basel.

Entities:  

Mesh:

Substances:

Year:  2001        PMID: 11408757     DOI: 10.1159/000063458

Source DB:  PubMed          Journal:  Horm Res        ISSN: 0301-0163


  2 in total

1.  Isolated haploinsufficiency of exon 1 of the SHOX gene in a patient with idiopathic short stature.

Authors:  Y-M Tan; K-Y Loke
Journal:  J Clin Pathol       Date:  2006-07       Impact factor: 3.411

2.  Retinoic acid catabolizing enzyme CYP26C1 is a genetic modifier in SHOX deficiency.

Authors:  Antonino Montalbano; Lonny Juergensen; Ralph Roeth; Birgit Weiss; Maki Fukami; Susanne Fricke-Otto; Gerhard Binder; Tsutomu Ogata; Eva Decker; Gudrun Nuernberg; David Hassel; Gudrun A Rappold
Journal:  EMBO Mol Med       Date:  2016-12-01       Impact factor: 12.137

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.