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Bookmark or Share- Noonan syndrome - Symptoms and causes - Mayo ClinicNoonan syndrome is a genetic condition that stops typical development in various parts of the body. It can affect a person in several ways, including unusual facial features, short height, heart problems and other physical problems.
- Noonan Syndrome | Children's Hospital of PhiladelphiaNoonan syndrome is a genetic disorder characterized by short stature, distinctive facial features, heart defects, bleeding problems and skeletal abnormalities. Most individuals with Noonan syndrome have normal intelligence, but some may have special educational needs or intellectual disability. Noonan syndrome occurs in about 1 in 2,500 births.
- Noonan Syndrome (Leopard Syndrome): Causes & Outlook - Cleveland ClinicOverview. What is Noonan syndrome? Noonan syndrome is a genetic condition that can affect your child in many ways. While some children born with this condition have mild symptoms, others can have more issues. Symptoms typically include unusual facial features such as a tall forehead and wide-set eyes, lower-set ears and a shorter neck.
- Noonan syndrome - Diagnosis and treatment - Mayo ClinicTreatment. Although there's no cure for Noonan syndrome, treatments can help decrease its effects. The earlier a diagnosis is made and treatment begins, the greater the benefits. Treatment for Noonan syndrome depends on the symptoms and complications and how serious they are.
- Noonan syndrome - UpToDateNoonan syndrome (NS) is a common autosomal-dominant condition that is associated with short stature and congenital heart disease (CHD), most often pulmonic stenosis. It is clinically and genetically heterogeneous.
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