- 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: 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 Foundation | noonan syndrome
What is Noonan Syndrome? Noonan syndrome can impact nearly every system in the body, causing heart defects, bleeding issues, developmental delays, and more Despite its prevalence, research is still uncovering its complexities
- 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
- What Is Noonan Syndrome? Does My Child Have the Signs? - WebMD
Noonan syndrome is a rare genetic disorder If you have it, you might have certain identifiable facial features, short height, and unusual chest shape You may also have heart defects It can
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