Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/2540
Title: A rare association of interrupted aortic arch type C and microdeletion 22q11.2
Authors: Cuturilo, Goran
Drakulic, Danijela
Stevanović, Milena 
Jovanovic, Ida
Djukic, Milan
Miletic-Grkovic, Slobodanka
Atanaskovic-Markovic, Marina
Keywords: Interrupted aortic arch type C;Microdeletion in chromosome 22q11.2
Issue Date: Oct-2008
Journal: European Journal of Pediatrics
Abstract: 
Microdeletion 22q11.2 is associated with a variety of findings, and the most common are cardiac defects. It is very frequently associated with interrupted aortic arch (IAA) type B and very rarely with type A and type C. Here we report the first case of IAA type C associated with 22q11.2 deletion in Serbia and, to the best of our knowledge, the fourth case described worldwide so far. By this report we would like to point out that all patients with IAA type C who have additional features specific for 22q11.2 microdeletion syndrome should be screened for the presence of this deletion. © 2007 Springer-Verlag.
URI: https://biore.bio.bg.ac.rs/handle/123456789/2540
ISSN: 0340-6199
DOI: 10.1007/s00431-007-0632-7
Appears in Collections:Journal Article

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