Fetal hemivertebra: a rare form of 18q deletion prenatal presentation

BMJ Case Rep. 2023 Feb 10;16(2):e251914. doi: 10.1136/bcr-2022-251914.

Abstract

The 18q deletion is a rare condition with several described features. A common phenotype includes short stature, microcephaly, facial defects, small feet, intellectual disability and hypotonia.We present a rare case of a fetus with del18q22.1q23 whose diagnosis was obtained by amniocentesis after a routine ultrasound at 20 weeks, where a hemivertebra was detected.Congenital hemivertebra is infrequent and is rarely associated with chromosomal anomalies. Expectant management can be advocated in isolated hemivertebra. This report shows that a hemivertebra can be an isolated prenatal finding in del18 so it is important to screen for, and exclude, chromosomal anomalies.

Keywords: Genetic screening / counselling; Pregnancy.

Publication types

  • Case Reports

MeSH terms

  • Amniocentesis
  • Chromosome Aberrations
  • Chromosome Deletion
  • Chromosome Disorders*
  • Female
  • Fetus
  • Humans
  • Pregnancy
  • Prenatal Diagnosis
  • Spinal Diseases*
  • Ultrasonography, Prenatal