Ventricular septal defect and deletion of chromosome 22q11: Anatomical types and aortic arch anomalies

Alessandra Toscano, Silvia Anaclerio, Maria Cristina Digilio, Aldo Giannotti, Giuseppe Fariello, Bruno Dallapiccola, Bruno Marino

Research output: Contribution to journalArticle

14 Citations (Scopus)

Abstract

In Caucasian children with ventricular septal defect and chromosome 22 deletions, the perimembranous type is the more frequent but the subarterial type and positional anomalies of the aortic arch are prevalent in comparison with patients with non-syndrome forms of ventricular septal defect.

Original languageEnglish
Pages (from-to)116-117
Number of pages2
JournalEuropean Journal of Pediatrics
Volume161
Issue number2
DOIs
Publication statusPublished - 2002

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Chromosome Deletion
Ventricular Heart Septal Defects
Thoracic Aorta
Chromosomes, Human, Pair 22

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

Cite this

Ventricular septal defect and deletion of chromosome 22q11 : Anatomical types and aortic arch anomalies. / Toscano, Alessandra; Anaclerio, Silvia; Digilio, Maria Cristina; Giannotti, Aldo; Fariello, Giuseppe; Dallapiccola, Bruno; Marino, Bruno.

In: European Journal of Pediatrics, Vol. 161, No. 2, 2002, p. 116-117.

Research output: Contribution to journalArticle

Toscano, Alessandra ; Anaclerio, Silvia ; Digilio, Maria Cristina ; Giannotti, Aldo ; Fariello, Giuseppe ; Dallapiccola, Bruno ; Marino, Bruno. / Ventricular septal defect and deletion of chromosome 22q11 : Anatomical types and aortic arch anomalies. In: European Journal of Pediatrics. 2002 ; Vol. 161, No. 2. pp. 116-117.
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