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Congenital heart disease in the 48,XXYY syndrome
D Meschede1, T Nekarda, D Kececioglu
1Institute of Human Genetics, University, Münster, Germany.
Clinical Genetics
|August 1, 1995
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.