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Down Syndrome Write for UsDown Syndrome Write for Us – Faulty cell division produces a second whole or incomplete copy of chromosome 21, which causes the genetic disorder known as Down syndrome. This unique genetic material causes the physiological traits and developmental alterations associated with Down syndrome. Down syndrome varies in severity between individuals, causing lifelong intellectual disability and developmental delays. The most common genetic chromosomal disorder causes youngsters with learning difficulties. In addition, it contributes to further medical issues, including digestive and cardiac problems.

A better understanding of Down syndrome and early interventions can significantly increase the quality of life for children and adults with the disorder and help them lead fulfilling lives.

How many children are born with Down Syndrome?

The most frequent chromosomal disorder identified in the US is still Down syndrome. Over 6,000 infants with Down syndrome are born annually in the US. This indicates that around 1 in 700 children have Down syndrome.

Types of Down Syndrome

There are three types of Down syndrome. People often cannot tell each species apart without looking at the chromosomes because physical traits and behaviors are similar.

Trisomy 21: Trisomy 21.2 affects around 95% of individuals with Down syndrome. Instead of the usual two copies of chromosome 21, each cell in the body with this variant of Down syndrome has three copies. Down syndrome: This type accounts for a small percentage of people with Down syndrome (about 3%).2 This occurs when a different segment, or an entire extra chromosome 21, is present but is linked or “mutated” to a different chromosome rather than a unique 21 chromosome. Mosaic Down syndrome affects around 2% of people with Down syndrome.

Mosaic is a word that means combination or mixture. When a kid has mosaic Down syndrome, some cells contain three copies of chromosome 21, while others only have the standard two copies. Children with mosaic Down syndrome may have traits in common with other children. However, because some (or many) of their cells possess a certain number of chromosomes, they may show fewer signs of the disease.

Causes and Danger Signs

The physical characteristics and developmental difficulties that might be present in persons with Chromosome 21 have an extra copy, which causes Down syndrome. Researchers know that an extra chromosome is the cause of Down syndrome, but no one is clear on the exact etiology or the myriad of contributing factors.

The mother’s age is one factor that raises the chance of having a kid with Down syndrome. Women at least 35 years old when they start pregnant are more likely to develop Down syndrome than women who become pregnant at a younger age. 3-5 However, the majority of children with Down syndrome are born to mothers more youthful than 35 since there are more births among younger women


Down syndrome can be identified during pregnancy using screening and diagnostic testing, the two primary types of tests available. A screening test can inform the expectant mother and her healthcare practitioner of the likelihood of Down syndrome development throughout the pregnancy. Although screening tests are safer for the woman and the unborn child, they do not offer a conclusive diagnosis. Down syndrome can be more risky for the mother and growing baby, although diagnostic testing can typically determine whether or not a newborn has it. Nobody can foresee the full effects of Down syndrome on a kid; neither screening nor diagnostic tools can.

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