Exome sequencing in the assessment of congenital malformations in the fetus and neonate

Fionnuala Mone*, Elizabeth Quinlan-Jones, Andrew K Ewer, Mark D Kilby

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

Abstract

Major congenital anomalies are often associated with perinatal mortality, long-term morbidity and prolonged hospitalisation. Prenatal ultrasound remains the principle diagnostic test for many anomalies, but despite this up to one-third are only identified in the neonatal period. The primary step in determining underlying aetiology is to define accurately the phenotype by recognition of dysmorphology (both prenatally and postnatally). The potential introduction of next-generation sequencing, primarily through exome sequencing, into perinatal practice may improve the pathological diagnostic yield. However, clinicians must understand both the benefit and potential harms of this technology in facilitating the discovery of relevant pathogenic variants in the diagnosis and management of congenital malformations.

Original languageEnglish
Pages (from-to)F452-F456
JournalArchives of Disease in Childhood - Fetal and Neonatal Edition
Volume104
Issue number4
Early online date01 Feb 2019
DOIs
Publication statusPublished - 19 Jul 2019
Externally publishedYes

Bibliographical note

© Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ.

Keywords

  • Congenital Abnormalities/diagnosis
  • Female
  • Humans
  • Infant, Newborn
  • Pregnancy
  • Prenatal Diagnosis/methods
  • Sequence Analysis, DNA/methods
  • Whole Exome Sequencing/statistics & numerical data

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