Frontiers in Genetics (Mar 2022)

Case Report: A Paternal 20q13.2-q13.32 Deletion Patient With Growth Retardation Improved by Growth Hormone

  • Yu Liu,
  • Ying Yang,
  • Liming Chu,
  • Shuai Ren,
  • Ying Li,
  • Aimin Gao,
  • Jing Wen,
  • Wanling Deng,
  • Yan Lu,
  • Lingyin Kong,
  • Bo Liang,
  • Xiaoshan Shao

DOI
https://doi.org/10.3389/fgene.2022.859185
Journal volume & issue
Vol. 13

Abstract

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Interstitial chromosome 20q deletions, containing GNAS imprinted locus, are rarely reported in the past. Hereby, we presented a Chinese boy with a novel 4.36 Mb deletion at paternal 20q13.2-13.32, showing feeding difficulty, malnutrition, short stature, lower limb asymmetry, sightly abnormal facial appearance and mild intellectual abnormality. With 3 years’ growth hormone treatment, his height was increased from 90 to 113.5 cm. This report is the first time to describe the outcome of clinical treatment on a patient with this rare chromosomal 20 long arm interstitial deletion, containing GNAS locus, which may facilitate the diagnosis and treatment of this type of patient in the future.

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