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

Masayuki Hasegawa, Heather H. Nelson, Edward Peters, Elin Ringstrom, Marshall Posner, Karl T. Kelsey

Research output: Contribution to journalArticlepeer-review

19 Scopus citations

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 (US)
Pages (from-to)116-117
Number of pages2
JournalEuropean Journal of Pediatrics
Volume161
Issue number2
DOIs
StatePublished - 2002

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