Noonan Syndrome is a rare genetic disorder that may be life-threatening but is highly treatable with regular medical care from a genetic disorder doctor and a team of specialists. What is Noonan Syndrome? Noonan Syndrome is a disorder caused by a genetic mutation. It may be inherited; children with a parent who has the condition
As a parent, you want the best for your child. When you hear that they might be diagnosed with a pediatric genetic disorder that impacts the course of their life, it can be stressful and emotional. Getting the facts right is critical to ensure that you can make informed decisions. What should parents understand about
Currently, more than 1200 genetic disorders are known to exist. With proper testing, doctors can identify most of these conditions in children. A genetic specialist can use several methods to diagnose chromosome disorders. These include biochemical testing, karyotyping, preimplantation genetic diagnosis, and neonatal genetic screening. How Can Genetics Help to Predict Diseases? Our genetic makeup