Noonan Syndrome is a genetic disorder that affects various parts of the body. It is characterized by distinctive facial features, short stature, heart defects, and developmental delays. The condition is caused by mutations in certain genes, which can be inherited or occur spontaneously. Individuals with Noonan Syndrome may also experience issues with blood clotting and have a higher risk of certain cancers. Diagnosis typically involves a physical examination and genetic testing. Early intervention and treatment can help manage symptoms and improve quality of life for those affected.