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Noonan syndrome is a genetic condition that stops typical development in various parts of the body People with ns may experience bleeding issues, congenital heart defects including hypertrophic cardiomyopathy and/or pulmonary valve stenosis, lymphatic abnormalities, small stature/growth issues, feeding and gastrointestinal issues, failure to thrive, hypertelorism. It can affect a person in several ways, including unusual facial features, short height, heart problems and other physical problems
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It also can cause a child to develop more slowly than usual, for example, in walking, talking or learning new things. Noonan syndrome is a rare disease in approximately 1 in 1000 to 1 in 2500 individuals. 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
Noonan syndrome is a genetic condition that can affect many parts of your child’s body
Early diagnosis and treatment can ease symptoms. Noonan syndrome (ns) is characterized by characteristic facies, short stature, congenital heart defect, and developmental delay of variable degree Other findings can include broad or webbed neck, unusual chest shape with superior pectus carinatum and inferior pectus excavatum, cryptorchidism, varied coagulation defects, lymphatic dysplasias, and ocular abnormalities 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. About noonan syndrome 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 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
