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Article Index
What Is Down Syndrome?
How Common is Down Syndrome?
Who is at Risk for Down Syndrome?
What is Chromosome 21?
What Are The Types of Down Syndrome?
Is Down Syndrome Inherited?
What Are The Characteristics of Down Syndrome?
What Other Health Problems Are Associated With Down Syndrome?
How is a Baby Tested for Down Syndrome?
How Commonly Are Down Syndrome Babies Aborted?
Is There a Cure for Down Syndrome?
What Medical Issues May I Encounter When Caring for a Newborn With Down Syndrome?
What Additional Care Does An Infant/Preschooler With Down Syndrome Need?
What Are Some Issues That Affect Adolescents and Adults with Down Syndrome?
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What is Down Syndrome?

Down syndrome, also called DS, is a condition caused by a mutation in the chromosomes during cell division. This mutation is a random event – it is not caused by environmental factors or by anything the parents did. In most people with Down syndrome, this mutation results in an extra copy of Chromosome 21. The extra genetic material disrupts the normal course of development of the body and the brain. Down syndrome is the most frequent genetic cause of mild to moderate developmental delay.



 
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