Down Syndrome with Complete Atrioventricular Septal Defect, Hypertrophic Cardiomyopathy, and Pulmonary Vein Stenosis

Author:

Mahadevaiah Guruprasad,Gupta Manoj,Ashwath Ravi

Abstract

The prevalence of congenital heart disease in infants with Down syndrome is 40%, compared with 0.3% in children who have normal chromosomes. Atrioventricular and ventricular septal defects are often associated with chromosomal aberrations, such as in trisomy 21, whereas hypertrophic cardiomyopathy is chiefly thought to be secondary to specific gene mutations. We found only one reported case of congenital hypertrophic cardiomyopathy and atrioventricular septal defect in an infant with Down syndrome. Here, we report atrioventricular septal defect, hypertrophic cardiomyopathy, and pulmonary vein stenosis in a neonate with Down syndrome—an apparently unique combination. In addition, we discuss the relevant medical literature.

Publisher

Texas Heart Institute Journal

Subject

Cardiology and Cardiovascular Medicine

Reference18 articles.

1. Congenital heart disease: prevalence at live-birth. The Baltimore-Washington Infant Study;Ferencz;Am J Epidemiol,1985

2. Unusual association of hypertrophic cardiomyopathy with complete atrioventricular canal defect and Down syndrome;Eidem;Tex Heart Inst J,2000

3. On the association of cardiac malformations with other congenital defects;Garrod;St Barth Hosp Rep,1894

4. Cardiovascular disease in Down syndrome;Spicer;Pediatr Clin North Am,1984

5. Increased adhesiveness of trisomy 21 cells and atrioventricular canal malformations in Down syndrome: a stochastic model;Kurnit;Am J Med Genet,1985

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