Guide To The Complications Of Noonan Syndrome

Noonan syndrome is a genetic condition that can cause differences in facial features and results in short stature. Patients with this syndrome frequently have cardiac issues such as irregular heart rhythms and thickening of the heart muscle, and they may also experience developmental delays. Blood tests can be performed to diagnose Noonan syndrome, and prenatal testing may be available too. Doctors might also suspect a diagnosis of Noonan syndrome after completing a physical exam. Since signs of the condition are subtle, some patients with Noonan syndrome do not get properly diagnosed until adulthood. Currently, the syndrome is estimated to occur in one out of every one thousand to 2,500 individuals. Treatment for the condition is tailored to the specific needs of each patient. Patients with heart problems are treated by cardiologists, and surgery may be necessary. Treatment with growth hormones may be appropriate for those with short stature, and early intervention and stimulation can help patients with learning differences. Of course, if treatment is not begun promptly, there is a risk of complications.