Noonan Syndrome Report

Noonan SyndromeThis report tests for mutations in genes associated with Noonan syndrome, a genetic disorder that affects many areas of the body. Noonan syndrome is characterized by characteristic facial features, short stature, heart defects, and developmental delays. Testing can help diagnose the condition, identify the genetic cause, and inform medical management and support for affected individuals and their families.More than 10 genes analyzed It is recommended if: Individuals who have symptoms of Noonan syndrome or a family history of the condition. This may include individuals with characteristic facial features, short stature, heart defects, or developmental delays. List of main conditions: