Pulmonary artery sling in a 22-month-old boy with 18q deletion syndrome: A rare but possible association

Angelica Bibiana Delogu*, Francesco Mariani, Francesca Graziani, Roberta Onesimo, Giancarlo Savino, Chiara Leoni, Giuseppe Zampino

*Autore corrispondente per questo lavoro

Risultato della ricerca: Contributo in rivistaArticolo

Abstract

The 18q deletion syndrome is a rare genetic condition characterized by a large variability in clinical phenotype and severity. Congenital heart diseases have been described by several previous reports, most commonly including pulmonary valve anomalies and septal defects. We describe a new case of a 22-month-old boy affected by 18q del syndrome found to have a symptomatic pulmonary artery sling. This study reports a new case of pulmonary artery sling associated with 18q del syndrome, providing an alert for pediatric cardiologists about less common cardiovascular anomalies, which can easily be missed, allowing for early diagnosis and appropriate care.
Lingua originaleInglese
pagine (da-a)741-744
Numero di pagine4
RivistaEchocardiography
Volume39
Numero di pubblicazione5
DOI
Stato di pubblicazionePubblicato - 2022

All Science Journal Classification (ASJC) codes

  • Radiologia, Medicina Nucleare e Diagnostica per Immagini
  • Cardiologia e Medicina Cardiovascolare

Keywords

  • 18q del syndrome
  • CT scan
  • Chromosome Deletion
  • Chromosome Disorders
  • Chromosomes
  • Congenital
  • Heart Defects
  • Human
  • Humans
  • Pair 18
  • Pulmonary Artery
  • Vascular Malformations
  • echocardiography
  • pulmonary artery sling

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