Congenital heart disease in the 48,XXYY syndrome
- 28 June 2008
- journal article
- case report
- Published by Wiley in Clinical Genetics
- Vol. 48 (2) , 100-102
- https://doi.org/10.1111/j.1399-0004.1995.tb04064.x
Abstract
We report on an infant with severe tetralogy of Fallot, bilateral preauricular pits, and a 48,XXYY chromosomal complement. This case and evidence collected from the literature suggest that congenital heart disease may occur in the 48,XXYY syndrome more frequently than currently appreciated.Keywords
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