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Bookmark or Share- Noonan Syndrome (Leopard Syndrome): Causes & Outlook - Cleveland ClinicNoonan syndrome occurs most often due to changes (mutations) in certain genes that help your body’s tissues grow and develop. These mutated genes produce proteins that are active longer than they should be.
- 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.
- Noonan Syndrome - StatPearls - NCBI BookshelfNoonan syndrome is a genetically inherited disease with heterogeneous, phenotypic manifestations. Gene mutations involve the RAAS/MAPK (mitogen-activated protein kinase) signaling pathway. The patient presentation can range from mild to severe.
- Noonan syndrome - Diagnosis and treatment - Mayo ClinicAlthough 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 - 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.
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