- 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 - StatPearls - NCBI Bookshelf
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-set ears, short stature, and pulmonic stenosis
- Noonan syndrome | About the Disease | GARD - Genetic and Rare Diseases . . .
Noonan syndrome is a genetic disorder that causes abnormal development of multiple parts of the body Features of Noonan syndrome may include a distinctive facial appearance, short stature, a broad or webbed neck, congenital heart defects, bleeding problems, problems with bone structure (skeletal malformations), and developmental delay
- 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 It is clinically and genetically heterogeneous
- 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 Early detection and treatment can ease symptoms and prevent complications What is Noonan syndrome?
- About Noonan Syndrome - National Human Genome Research Institute
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 bones of the rib cage
- 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
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