Noonan Syndrome: A Rare Genetic Disorder

Sailender15 Oct, 2020Health

Noonan syndrome is characterized by a broad spectrum of physical features that vary based on range and severity. Noonan syndrome is a rare condition generally caused by changes in one of the several autosomal dominant genes. It is present in about 1 in 1,000 or 1 in 2,500 people.