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Congenital heart disease and cardiac procedural outcomes in patients with trisomy 21 and Turner syndrome

Raysa Morales-Demori
Department of Pediatrics, Division of Pediatric Cardiology, Baylor College of Medicine, Texas Children’s Hospital, Houston, Texas, USA
* Corresponding Author: Raysa Morales-Demori, MD, Division of Pediatric Cardiology, Texas Children’s Hospital, 6621 Fannin st, MC 19345-C, Houston, TX 77030. Email:

Congenital Heart Disease 2017, 12(6), 820-827. https://doi.org/10.1111/chd.12521

Abstract

Congenital heart disease (CHD) is present in approximately 50% of patients with trisomy 21 (T21) and Turner syndrome (TS). According to the American Academy of Pediatrics, every patient with these genetic disorders should have a postnatal echocardiogram. T21 is usually associated with atrioventricular (30%–60%), atrial (16%-21%), or ventricular septal defects (14%–27%). TS is usually associated with left-sided heart disease. However, the spectrum of CHD in these genetic disorders is wider than those mentioned lesions. More cardiac surgical procedures are offered to these patients and that has influenced positively their life expectancy for some CHD conditions. Single ventricular anatomy is associated with high mortality in these genetic disorders (49% in T21 and 83%–91% in TS). The goal of this article is to describe the spectrum of CHD, screening guidelines, and cardiac surgical outcomes in patients with T21 or TS with CHD.

Keywords

congenital heart disease, outcomes, trisomy 21, Turner syndrome

Cite This Article

Morales-Demori, R. (2017). Congenital heart disease and cardiac procedural outcomes in patients with trisomy 21 and Turner syndrome. Congenital Heart Disease, 12(6), 820–827.



This work is licensed under a Creative Commons Attribution 4.0 International License , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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