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Noonans syndrome facial

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Metrics details. Noonan Syndrome NS is characterised by short stature, typical facial dysmorphology and congenital heart defects. The incidence of NS is estimated to be between and live births. The main facial features of NS are hypertelorism with down-slanting palpebral fissures, ptosis and low-set posteriorly rotated ears with a thickened helix.
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An Overview of Noonan Syndrome

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Noonan syndrome – a new survey

Back to Health to A-Z. Noonan syndrome is a genetic condition that can cause a wide range of distinctive features and health problems. The condition is present from before birth, although milder cases may not be diagnosed until a child gets older. It's estimated that between 1 in 1, and 1 in 2, children are born with Noonan syndrome. It affects both sexes and all ethnic groups equally.
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Noonan syndrome

Professional Reference articles are designed for health professionals to use. You may find one of our health articles more useful. NICE has issued rapid update guidelines in relation to many of these. This guidance is changing frequently. Noonan syndrome NS is a common genetic disorder with multiple congenital abnormalities.
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Chris Vincent, MD, is a licensed physician, surgeon, and board-certified doctor of family medicine. Designated as a rare disease, it is estimated that this condition affects approximately 1 out of to people. Noonan Syndrome is not associated with any particular geographic region or ethnic group.
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