- Noonan syndrome - Symptoms and causes - Mayo Clinic
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, heart problems and other physical problems
- Noonan syndrome - Wikipedia
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]
- Noonan syndrome | About the Disease | GARD - Genetic and Rare Diseases . . .
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 randomly when cells are dividing
- Noonan Syndrome (Leopard Syndrome): Causes Outlook
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 problems
- Noonan Syndrome | Childrens Hospital of Philadelphia
Noonan syndrome is a genetic disorder characterized by short stature, distinctive facial features, heart defects, bleeding problems, and skeletal abnormalities
- Noonan syndrome: MedlinePlus Genetics
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 many other signs and symptoms
- Noonan syndrome - UpToDate
Noonan syndrome (NS) is a common autosomal-dominant condition that is associated with short stature and congenital heart disease (CHD), most often pulmonic stenosis
- Noonan Syndrome: What Is It, Causes, Treatment and More | Osmosis
Noonan syndrome is a congenital genetic disorder that prevents typical development in many areas of the human body, leading to a wide range of distinctive physical features and health conditions, such as facial characteristics, short stature, heart defects, and developmental delays
|