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, short height, …

Noonan syndrome is a condition that affects many areas of the body. It is characterized by mildly unusual facial features, short stature, heart defects, bleeding problems, skeletal malformations, and …

Noonan syndrome is caused by genetic mutations, also known as pathogenic variants. Genetic mutations can be hereditary, when parents pass them down to their children, or they may occur …

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 stature and heart …

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

Noonan syndrome is a genetic disorder associated with a number of physical abnormalities, including short stature, heart defects, and an abnormal appearance.

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 malformations of the …

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

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