Deletion 22q11 in patients with interrupted aortic arch

Bruno Marino; Maria Cristina Digilio; Monica Persiani; Roberto Di Donato; Alessandra Toscano; Aldo Giannotti; Bruno Dallapiccola

doi:10.1016/S0002-9149(99)00297-0

Deletion 22q11 in patients with interrupted aortic arch

Bruno Marino, Maria Cristina Digilio, Monica Persiani, Roberto Di Donato, Alessandra Toscano, Aldo Giannotti, Bruno Dallapiccola

Ospedale Pediatrico Bambino Gesu

Research output: Contribution to journal › Article

Abstract

In our series of 27 children with various types of interruption of the aortic arch (IAA), deletion 22q11 is prevalent in patients with simple IAA type B, and is absent in patients with IAA type A and in those with associated additional major cardiac defects. Anomalies of the infundibular septum should be considered a characteristic aspect of children with IAA and deletion 22q11.

Original language	English
Pages (from-to)	360-361
Number of pages	2
Journal	The American Journal of Cardiology
Volume	84
Issue number	3
DOIs	https://doi.org/10.1016/S0002-9149(99)00297-0
Publication status	Published - Aug 1 1999

ASJC Scopus subject areas

Cardiology and Cardiovascular Medicine

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Marino, B., Digilio, M. C., Persiani, M., Di Donato, R., Toscano, A., Giannotti, A., & Dallapiccola, B. (1999). Deletion 22q11 in patients with interrupted aortic arch. The American Journal of Cardiology, 84(3), 360-361. https://doi.org/10.1016/S0002-9149(99)00297-0

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AU - Dallapiccola, Bruno

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