Overview

Aortic coarctation (ko-ahrk-TAY-shun) is a narrowing of part of the aorta. The aorta is the main artery of the body. Aortic coarctation also is called coarctation of the aorta.

The condition forces the heart to work harder to pump blood.  It usually is present at birth. That means it is a congenital heart defect. But sometimes the condition can occur later in life.

Coarctation of the aorta often occurs along with other congenital heart defects. Treatment to fix the condition is usually successful. But regular health checkups are needed for life to watch for changes in the heart's health.

Symptoms

Symptoms of coarctation of the aorta depend on how much of the aorta is narrowed. Most people don't have symptoms.

Adults and older children with mild coarctation of the aorta may not have symptoms. Their hearts may seem healthy.

If a baby is born with an extreme narrowing of the aorta, symptoms may be seen shortly after birth. Symptoms of coarctation of the aorta in infants include:

  • Trouble breathing.
  • Trouble feeding.
  • Heavy sweating.
  • Irritability.
  • Blue or gray skin, lips and fingernails. Depending on the skin color, these changes may be harder or easier to see.

Symptoms of coarctation of the aorta later in life may include:

  • Chest pain.
  • High blood pressure.
  • Headaches.
  • Muscle weakness.
  • Leg cramps.
  • Cold feet.
  • Nosebleeds.

Coarctation of the aorta often occurs with other heart conditions present at birth. Other symptoms depend on the types of congenital heart defects.

When to see a doctor

Always get medical help right away for chest pain that is sudden or not explained.

Also get medical help for these symptoms:

  • Fainting.
  • Sudden shortness of breath.
  • High blood pressure that can't be explained.

Many different health conditions can cause these symptoms. A complete health checkup is needed to learn the cause.

Causes

The cause of coarctation of the aorta is not clear. It's usually a heart condition present at birth, called a congenital heart defect. A congenital heart defect happens as the baby, called a fetus, is growing in the womb during pregnancy. The cause is often not known.

Rarely, coarctation of the aorta can happen later in life. Conditions or events that can narrow the aorta and cause this condition include:

  • Traumatic injury.
  • A buildup of fats, cholesterol and other substances in and on the artery walls, called atherosclerosis.
  • A rare type of swelling and irritation of blood vessels in the heart, called Takayasu arteritis.

Risk factors

Risk factors for coarctation of the aorta include:

  • Male sex.
  • Some genetic conditions, such as Turner syndrome.
  • Some heart conditions present at birth, called congenital heart defects.

Congenital heart defects that can occur with coarctation of the aorta include:

  • Bicuspid aortic valve. The aortic valve is between the lower left chamber of the heart and the aorta, which is the body's main artery. Typically, the aortic valve has three cusps. A bicuspid aortic valve has only two cusps.
  • Subaortic stenosis. This is a narrowing of the area below the aortic valve. It blocks blood flow from the lower left heart chamber to the aorta.
  • Patent ductus arteriosus. The ductus arteriosus is a blood vessel that connects the lung arteries to the aorta. When a baby is growing in the womb, this vessel lets blood go around the lungs. Shortly after birth, the ductus arteriosus usually closes. If it stays open, it's called a patent ductus arteriosus.
  • Holes in the heart. Some people with coarctation of the aorta also are born with a hole in the heart. If the hole is between the upper heart chambers, it is called an atrial septal defect. A hole between the lower heart chambers is called a ventricular septal defect.
  • Congenital mitral valve stenosis. This is a type of heart valve disease that some people are born with. The valve between the upper and lower left heart chambers is narrowed or small. It's harder for blood to move through the valve.

Complications

Complications of coarctation of the aorta happen because the lower left heart chamber has to work harder to pump blood through the narrowed artery. This makes blood pressure go up in the lower left heart chamber. Also, the wall of the chamber can get thick. This condition is called ventricular hypertrophy.

Complications of coarctation of the aorta include:

  • A bulge in the wall of the aorta, called an aortic aneurysm.
  • A bulge or ballooning in a blood vessel in the brain, also known as a brain aneurysm.
  • A rupture or tear in the aorta, called an aortic dissection.
  • Bleeding in the brain.
  • Coronary artery disease.
  • High blood pressure that doesn't go away. Blood pressure usually drops after surgery to fix the aorta, but it may still be higher than usual.
  • Stroke.

Treatment may be needed right away to prevent complications. Without treatment, coarctation of the aorta may lead to:

  • Kidney failure.
  • Heart failure.
  • Death.

Some people have complications after treatment for coarctation of the aorta. These complications include:

  • Repeat narrowing of the aorta, called recoarctation.
  • Aortic aneurysm or rupture.

To prevent complications, people with coarctation of the aorta need regular health checkups for life.

Prevention

There's no known way to prevent coarctation of the aorta. Tell your healthcare team if anyone in your family was born with a heart condition.

Aug. 15, 2026

Living with coarctation of the aorta?

Connect with others like you for support and answers to your questions in the Heart & Blood Health support group on Mayo Clinic Connect, a patient community.

Heart & Blood Health Discussions

Nazir Khan
Statin discontinued due to neuropathy. What are some alternatives?

454 Replies Thu, Aug 13, 2026

lpyne
Fibromuscular dysplasia (FMD): Want to connect

133 Replies Tue, Aug 11, 2026

Becky, Volunteer Mentor
The Patient Portal—Help or Hindrance?

255 Replies Wed, Aug 05, 2026

See more discussions
  1. Coarctation of the aorta. American Heart Association. https://www.heart.org/en/health-topics/congenital-heart-defects/about-congenital-heart-defects/coarctation-of-the-aorta-coa. Accessed April 29, 2026.
  2. Hijazi ZM, et al. Clinical manifestations and diagnosis of coarctation of the aorta. https://www.uptodate.com/contents/search. Accessed April 29, 2026.
  3. Gurvitz M, et al. 2025 ACC/AHA/HRS/ISACHD/SCAI guideline for the management of adults with congenital heart disease: A report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines. Circulation. 2025; doi:10.1161/CIR.0000000000001402.
  4. AskMayoExpert. Coarctation of the aorta. Mayo Clinic; 2025.
  5. Goldman L, et al., eds. Congenital heart disease in adults. In: Goldman-Cecil Medicine. 27th ed. Elsevier; 2024. https://www.clinicalkey.com. Accessed May 3, 2026.
  6. Ferri FF. Coarctation of the aorta. In: Ferri's Clinical Advisor 2026. Elsevier; 2026. https://www.clinicalkey.com. Accessed May 4, 2026.
  7. Marcdante KJ, et al., eds. Acyanotic congenital heart disease. In: Nelson Essentials of Pediatrics. 9th ed. Elsevier; 2023. https://www.clinicalkey.com. Accessed May 4, 2026.
  8. Stout KK, et al. 2018 AHA/ACC guideline for the management of adults with congenital heart disease: Executive summary: A report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines. Journal of the American College of Cardiology. 2019; doi:10.1016/j.jacc.2018.08.1028.
  9. Bacha E, et al. Management of coarctation of the aorta. https://www.uptodate.com/contents/search. Accessed May 4, 2026.
  10. Life's Essential 8. American Heart Association. https://www.heart.org/en/healthy-living/healthy-lifestyle/lifes-essential-8. Accessed May 6, 2026.