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. Author manuscript; available in PMC: 2014 Sep 4.
Published in final edited form as: Am J Med Genet B Neuropsychiatr Genet. 2013 Nov 22;0(2):137–147. doi: 10.1002/ajmg.b.32215

TABLE II.

CHD Phenotype of Participants With CHD-Only, 22q-noCHD, and 22q-CHD

CHD-only 22q-noCHD 22q-CHD P-value
CHD phenotype 0.02
 Tetralogy of fallot (%) 6 (38) 7 (26)
 Interrupted aortic arch (%) 1 (6) 6 (22)
 Ventricular septal defect (%) 9 (56) 2 (7)
 Truncus arteriosus (%) 0 5 (19)
 Patent ductus arteriosus (%) 0 4 (15)
 Atrial septal defect (%) 0 2 (7)
 Biscuspid aortic valve (%) 0 1 (4)
Other vascular anomaliesa NS
 yes (%) 11 (40) 19 (70)
 no (%) 8 (30) 5 (19)
 unknown (%) 16 (100) 8 (30) 3 (11)
CHD surgery (%) 16 (100) 21 (78) NS

P-values are determined by Fisher’s exact test. NS designates non-significance (P > 0.05).

a

Includes vascular ring, right aortic arch with mirror-image branching of brachiocephalic vessels, and aberrant origin subclavian artery.