Overview

Hypoplastic left heart syndrome (HLHS) is a rare heart condition that a child is born with. That means it's a congenital heart defect. In this condition, the left side of the heart doesn't develop fully and is too small. So it can't pump blood well. Instead, the right side of the heart must pump blood to the lungs and to the rest of the body.

Treatment for hypoplastic left heart syndrome may include medicines, heart surgery or a heart transplant. Advances in care have improved the outlook for babies born with HLHS.

Symptoms

Babies born with hypoplastic left heart syndrome (HLHS) usually are very sick soon after birth. Symptoms of HLHS include:

  • Blue or gray skin, lips or fingernails. Depending on skin color, these changes may be harder or easier to see.
  • Rapid, difficult breathing.
  • Poor feeding.
  • Cold hands and feet.
  • Weak pulse.
  • Being more drowsy or less active than is typical for most babies.

Without treatment, a baby with this condition may go into shock. Symptoms of shock include:

  • Cool, clammy skin that can be pale or lips that can be blue or gray.
  • A weak and rapid pulse.
  • Breathing that may be slow and shallow or very rapid.
  • Dull eyes that seem to stare.

When to see a doctor

Get emergency medical help if your baby has:

  • Changes in skin or nail color.
  • Trouble breathing or fast breathing.
  • Weak pulse or rapid pulse.
  • Cool clammy skin.

Causes

Hypoplastic left heart syndrome (HLHS) happens in the womb when a baby's heart develops. The cause isn't known. Gene changes may play a role.

In hypoplastic left heart syndrome, the left side of the heart hasn't grown enough so it does not develop fully. It can't properly send blood to the body. In HLHS, the following areas of the heart are too small:

  • The lower left heart chamber, called the left ventricle.
  • The body's main artery, called the aorta.
  • The heart valves on the left side of the heart, called the aortic and mitral valves.

After birth, the right side of a baby's heart usually pumps blood both to the lungs and to the rest of the body. The blood passes through an opening called the ductus arteriosus. This opening, also called a vessel, connects the pulmonary artery directly to the aorta. The oxygen-rich blood goes back to the right side of the heart through a natural opening between the right chambers of the heart. The opening is called the foramen ovale.

The ductus arteriosus usually closes after the first day or two of life. When that happens, the right side of the heart has no way to pump blood to the body. The left side of the heart takes over this job.

But in babies with hypoplastic left heart syndrome, the left side can't pump blood well. So they need medicine to keep these connections open and keep blood flowing to the body until they have heart surgery.

Risk factors

People who have a child with hypoplastic left heart syndrome (HLHS) have a higher risk of having another baby with this or a similar condition.

There are no other clear risk factors for hypoplastic left heart syndrome.

Complications

With proper treatment, many babies with hypoplastic left heart syndrome (HLHS) survive. But they do need many surgeries and can have less energy and other challenges. Complications of HLHS may include:

  • Getting tired more easily during sports or other exercises.
  • Irregular heartbeats, called arrhythmias.
  • Fluid buildup, called edema, in the lungs, stomach area, legs and feet.
  • Not growing well.
  • Developmental conditions related to the brain and nervous system.
  • Need for more heart surgery or a heart transplant.

Prevention

There's no way to prevent hypoplastic left heart syndrome. If you were born with a heart condition, talk with a heart doctor and genetic counselor before getting pregnant.

By Mayo Clinic Staff