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

Risultato della ricerca: Contributo in rivistaArticolo in rivista

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 originaleEnglish
pagine (da-a)741-744
Numero di pagine4
RivistaEchocardiography
Volume39
DOI
Stato di pubblicazionePubblicato - 2022

Keywords

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

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