Noonan syndrome

Noonan syndrome can be inherited in an autosomal dominant manner. It affects at least 1 in 2,500 children.
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Noonan syndrome may result from excessive SHP-2 activity. Typical features include abnormalities of the heart.
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NS: Noonan syndrome, a multifaceted condition characterized by a series of birth defects (congenital malformations) including short stature after birth (postnatal growth retardation), webbing of the neck (pterygium colli), ...
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Some syndromes that include congenital heart disease (not all cyanotic) are Down syndrome, trisomy 13, Turner's syndrome, Marfan syndrome, Noonan syndrome, and Ellis-van Creveld syndrome.
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diseases occur as an isolated defect and are not associated with other diseases. However, they can also be a part of various genetic and chromosomal syndromes, such as Down syndrome, trisomy 13, Turner's syndrome, Marfan syndrome, Noonan syndrome, ...
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