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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 (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 - Wikipedia A number of diverse gastrointestinal (GI) symptoms have been associated with Noonan syndrome These include swallowing difficulties, low gut motility, gastroparesis (delayed gastric emptying), intestinal malrotation, and frequent or forceful vomiting
Noonan Syndrome - GeneReviews® - NCBI Bookshelf Noonan syndrome (NS) is characterized by characteristic facies, short stature, congenital heart defect, and developmental delay of variable degree
Noonan syndrome - MedlinePlus 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: Symptoms, Diagnosis, Treatment, and More People with Noonan syndrome may have certain facial features, heart defects, short stature, or other physical and developmental issues Since signs and symptoms can vary greatly from person
Noonan Syndrome | Symptoms, Diagnosis Treatment Noonan syndrome is a genetic condition with an incidence of 1 in 1,000 to 1 in 2,500 live births Common features of the condition include congenital heart disease, short stature, distinctive facial features, bleeding disorders and learning disabilities
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