Article Text

Download PDFPDF
Short stature? Call the geneticist

Statistics from

Request Permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

Next generation sequencing technologies (NGS) such as exome sequencing (ES) and chromosomal microarray analysis (CMA) didn’t exist when Archivist was at medical school. There are now several well recognised genetic factors contributing to short stature including traditional chromosomal abnormalities but also copy number variations (CNVs), and single-nucleotide variants. How do these new tools help in making a diagnosis? What is the yield? Currently it is unclear. Li Q et al [JAMA Pediatr 2023;177:1149–57. doi:10.1001/jamapediatrics.2023.3566] have completed a systematic review and metanalysis to examine the value of CMA and ES. They have interrogated 5222 studies and after screening of the abstracts and …

View Full Text


  • Provenance and peer review Commissioned; internally peer reviewed.