Fallot's Tetralogy Report

Fallot's TetralogyFallot's tetralogy is a congenital heart defect characterized by four anatomical abnormalities in the heart, including a hole in the wall between the heart's chambers and narrowing of the pulmonary artery. This report screens for genetic variants associated with Fallot's tetralogy and related conditions, such as pulmonary atresia and double outlet right ventricle. These conditions can cause symptoms such as cyanosis (blue-tinted skin), shortness of breath, and poor growth, and can lead to complications such as heart failure and arrhythmias.More than 120 genes analyzed It is recommended if: This report is useful for individuals with a family history of congenital heart defects or individuals with symptoms such as cyanosis, shortness of breath, or poor growth. Early diagnosis can inform treatment and management strategies, such as surgical interventions or medication. List of main conditions: Fallot's Tetralogy