Noonan syndrome is a rare genetic disorder. If you have it, you might have certain identifiable facial features, short height, and unusual chest shape. You may also have heart defects. It can ...

At initial assessment, mild developmental delay was noted. Noonan syndrome was suspected. Echocardiography showed a small perimembranous VSD and nonobstructive HCM with mild mitral valve prolapse.

Noonan syndrome is a genetic disorder that prevents normal development in the body. A person can be affected by Noonan syndrome in various ways such as with unusual facial characteristics ...

Worried, her parents took her to the emergency room. There doctors discovered that Maria, who at age 2 was diagnosed with Noonan syndrome, a genetic disorder that can lead to several health issues ...

Noonan syndrome is a genetic disorder that affects ... Normal cardiac function was restored after medication and treatment. An echocardiogram revealed a structurally normal heart with normal ...

Noonan syndrome is a genetic condition that affects around 1 in every 1,000–2,500 people. The signs and symptoms can vary greatly from person to person, so this condition may be underdiagnosed ...

Noonan syndrome is a condition that produces characteristic physical traits (eye shape, for example) and contributes to the risk of conditions like heart disease, bleeding disorders, and other ...