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Atrial Heart Septal Defect 3
An atrial heart septal defect type 3 that is caused by heterozygous mutation in the myosin heavy chain-6 gene (MYH6) on chromosome 14q12.
This information is for educational purposes only and is not medical advice. Always consult your healthcare provider about your specific condition and treatment.
When to seek help
Seek medical help right away if you have severe, sudden, or worsening symptoms, trouble breathing, chest pain, or any symptom that feels life-threatening. This community is for peer support and education only and is not a substitute for professional medical advice.
If you are experiencing a medical emergency, contact your local emergency services immediately.
Overview
What are congenital heart defects? Congenital heart defects (CHDs) are problems with the structure of the heart. "Congenital" means that that the problems are present at birth. These defects happen when a fetus's heart doesn't develop normally during pregnancy. Congenital heart defects are the most common type of birth defect. Congenital heart defects can change the way the heart pumps blood. They may make blood flow too slowly, go the wrong way, or block it completely. There are many types of congenital heart defects. They can happen in one or more parts of the heart. The most common types are: Septal defects ( "hole in the heart") - openings in the wall between the left and right…
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Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.