Fallot's Tetralogy Report
Fallot's Tetralogy
Fallot'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
Simple workflow
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FAQs
How will my data be used?
Your data is yours. Which is why we have developed proprietary software linked to a dedicated platform, the Genome Manager, to provide you with unique access to your data whenever you want, wherever you are.
How can my doctor use the results?
You will be provided with a digital version of the raw data and reports. Thanks to these in-depth tools, you will be able to share your preferred information with your geneticist and/or doctor to indicate and plan the healthiest course for you.
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*Raw data will be available free of charge for the first 30 days after release.
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