Short stature homeobox-containing gene duplications in 3.7% of girls with tall stature and normal karyotypes

Acta Paediatr. 2017 Oct;106(10):1651-1657. doi: 10.1111/apa.13969. Epub 2017 Jul 20.

Abstract

Aim: The short stature homeobox-containing gene (SHOX) plays an important role in short stature, but has not been explored in detail in a tall stature population before. This study explored the prevalence of SHOX aberrations in girls diagnosed with idiopathic tall stature with a normal karyotype.

Methods: We studied SHOX aberrations in 81 girls with a median age of 10.43 (7.17-12.73) years diagnosed with tall stature who were referred to our clinic at Copenhagen University Hospital, Denmark, between 2003 and 2013. SHOX copy variations were analysed by quantitative polymerase chain reaction, and aberrations were confirmed by multiplex ligation probe-dependent amplification.

Results: One extra SHOX copy was found in three (3.7%) of the 81 girls with tall stature, and their heights were 2.87, 3.71 and 3.98 standard deviation scores (SDS) and above the median height SDS of the girls with two SHOX copies. Their sitting height/height ratios (-3.08, -2.00 and -2.18 SDS) were all lower than the population mean. Despite these SHOX duplications, the three girls were clinically and biochemically comparable to the 78 girls with two SHOX copies.

Conclusion: This study was the first to demonstrate SHOX duplications in three girls with tall stature and normal karyotypes.

Keywords: Girls; Height; Short stature homeobox-containing gene; Tall stature.

MeSH terms

  • Adolescent
  • Body Height / genetics*
  • Child
  • Cohort Studies
  • Female
  • Humans
  • Karyotype
  • Short Stature Homeobox Protein / genetics*

Substances

  • SHOX protein, human
  • Short Stature Homeobox Protein