It can cause a wide range of other physical and developmental symptoms that usually start at birth.
There’s no cure for it, but doctors can treat some of the symptoms as they happen.
What Causes It?
Noonan syndrome is caused by a genetic defect. Scientists have identified four genes involved in the syndrome: PTPN11, SOS1, RAF1, and KRAS.
There are two ways you can get this syndrome:
- The gene mutation is passed down to you by one parent
- The altered gene happens for the first time while you are still in the womb
What Are the Symptoms?
There are many symptoms, and they may be mild, moderate, or severe.
Head, Face, and Mouth
Bones and Chest
- Short height (about 70% of patients)
- Either sunken or protruding chest
- Low-set nipples
Most babies with Noonan syndrome are also born with heart disease. They may have:
- Narrowing of the valve that moves blood from the heart to the lungs
- Swelling and weakening of the heart muscle
- Atrial septal defects
- Delayed puberty
- Testes that don’t descend -- this can cause infertility
How’s It Diagnosed?
Your doctor might also suspect Noonan syndrome if you have abnormal results on a specialized prenatal test, called a maternal serum triple screen.
Most of the time, they’ll know your baby has this condition at birth or shortly after by examining them. But sometimes, it’s hard to recognize and diagnose.
What’s the Treatment?
There isn’t one. But your doctor will prescribe treatments for your baby’s symptoms or complications. For example, growth hormones may help with growth problems.
What Else Should I Know?
If you have Noonan syndrome, you may wonder if your future children will have it. That depends on your family’s history
If one of your parents has the condition, they have a 50% chance of passing it on to you.
But if you have Noonan syndrome and no one else in your family had it, the defective gene may have started with you. Doctors call this a “de novo mutation.” In this case, your chances of passing it along to a future child are very small -- less than 1%.
If you’re concerned, see a genetic specialist. They can run tests to spot mutations that happen with this syndrome, and help confirm whether your child has it or not.