Noonan syndrome (NS) is a genetic disorder that may present with mildly unusual facial features, short height, congenital heart disease, bleeding problems, and skeletal malformations. [1]

May 25, 2023 · Noonan 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, …

Noonan syndrome is typically a genetically inherited disorder with heterogeneous phenotypic manifestations that can change with age. The most consistent features are wide-set eyes, low …

Dec 16, 2024 · Noonan syndrome is a genetic disorder characterized by short stature, distinctive facial features, heart defects, bleeding problems, and skeletal abnormalities.

Jan 27, 2023 · Noonan syndrome is a genetic condition that can affect many parts of your child’s body. While symptoms vary widely, they most often include unusual facial features, short …

To confirm the diagnosis of Noonan syndrome, genetic tests are done on samples of blood. There is no cure for Noonan syndrome. However, some specific symptoms and problems caused by …

Learn what it means to have Noonan Syndrome, what to expect, and how to manage the diagnosis.

Dec 23, 2013 · Noonan syndrome is a disorder that involves unusual facial characteristics, short stature, heart defects present at birth, bleeding problems, developmental delays, and …

Nov 15, 2001 · Noonan syndrome (NS) is characterized by characteristic facies, short stature, congenital heart defect, and developmental delay of variable degree.

Find out about Noonan syndrome, including the features and problems, causes, how it's diagnosed and the treatment and support available.