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Fig. 4 | Cell & Bioscience

Fig. 4

From: Incidence, distribution, disease spectrum, and genetic deficits of congenital heart defects in China: implementation of prenatal ultrasound screening identified 18,171 affected fetuses from 2,452,249 pregnancies

Fig. 4

Karyotyping of fetal CHD. Trisomy 18 was identified as the most common chromosomal abnormality in fetal CHD, followed by trisomy 21. AA, aortic atresia. ADV, . AS, aortic stenosis. ASD, atrial septal defect. CVR, congenital vascular ring. DORV, double-outlet right ventricle. ECD, endsystolic dimension. HLHS, hypoplastic left heart syndrome. HRHS, hypoplastic right heart syndrome. HS, heterotaxy syndrome. IAA, interrupted aortic arch. MA, mitral atresia. PA, pulmonary atresia. PLSVC, persistent left superior vena cava. PS, pulmonary stenosis. PTA, persistent truncus arteriosus. SV, single ventricle. TGA, transposition of the great arteries. TOF, tetralogy of Fallot. TVD, tricuspid valve disease. VSD, ventricular septal defect

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Cell & Bioscience

ISSN: 2045-3701

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