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Double aoRTIC aRCh: an unCommon Cause of sTRIDoR In an InfanT
2015
The Journal of Cardiovascular Diseases
unpublished
Preserved Fulltext
A male infant six months of age presented with stridor. Echo, MRI, cardiac catheterization confirmed the diagnosis of double aortic arch. The child underwent successful surgery. The case is reported as an uncommon cardiac anomaly and an uncommon cause of stridor in an infant.
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