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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 | 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 (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
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
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
Noonan Syndrome - novoMEDLINK Noonan syndrome is named for Dr Jacqueline Noonan, a pediatric cardiologist, who first identified it in 1962 Noonan syndrome is caused by a genetic mutation that may cause congenital heart disease, distinctive facial features, short stature, and other conditions