Noonan Syndrome a genetic condition

Noonan Syndrome (NS) is a genetically heterogenous autosomal dominant condition associated with short stature, variable intellectual capacity, neck webbing and ocular hypertelorism (abnormally increased distance between the orbits). There is also a strong association with congenital heart disease most often pulmonic stenosis and hypertrophic cardiomyopathy (in 20%).
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easy to understand

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