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    Noonan Syndrome

    Noonan syndrome is a condition that produces characteristic physical traits (eye shape, for example) and contributes to the risk of conditions like heart disease, bleeding disorders, and other health challenges.

    It affects approximately one out of 1,000 to 2,500 people. 

    Noonan syndrome is a genetic disorder, but not all cases are inherited. It is not associated with any particular ethnic group. While life expectancy with Noonan syndrome is typical and the condition is not life-threatening, the associated health problems are expected later in life.

    This article discusses Noonan syndrome symptoms and its causes.

    Noonan syndrome personality

    It explains how Noonan syndrome is diagnosed and treated, and why careful health monitoring can help to limit the worst impacts.

    What Is Noonan Syndrome?

    Noonan syndrome is an autosomal dominant genetic disease, which means that if one parent has the disease, then the child will also have the disease.

    There are instances of sporadic Noonan syndrome, which means that the genetic abnormality behind it can arise in a child who did not

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