Our commitment to keeping you safe

We have never taken for granted the sacred trust you place in us to care for your child, and today we are more grateful than ever for that privilege. To learn about all the ways we are working to keep you, your family and our team members safe, visit our COVID-19 updates page.

Pediatric Noonan Syndrome

Noonan syndrome is a genetic disorder that prevents normal growth and development.

What is Pediatric Noonan Syndrome?

Noonan syndrome is a genetic disorder that can be inherited from one or both parents. Noonan syndrome prevents normal development and causes many problems throughout a child’s body. The most common problems include heart conditions and skeletal malformations.

Risk factors

Your child is at risk for Noonan syndrome if one or both parents carry the defective gene.

What are the signs and symptoms of Pediatric Noonan Syndrome?

The most common symptoms of Noonan syndrome include:

What are the causes of Pediatric Noonan Syndrome?

Noonan syndrome is a genetic disorder, meaning that a gene inherited from one or both parents is defective. During fetal development, Noonan syndrome is caused by changes in one of several dominant genes.