During meiosis homologous chromosomes are separated and only one copy of each chromosome goes into the gamete. If they aren't separated correctly, both copies may go into the gamete. After fertilisation, the embryo will contain 3 copies of that chromosome. If this occurs with chromosome 21, it will result in Down Syndrome.
Normally, at the time of conception a baby inherits genetic information from its parents in the form of 46 chromosomes: 23 from the mother and 23 from the father. In most cases of Down syndrome, a child gets an extra chromosome 21 - for a total of 47 chromosomes instead of 46. It's this extra genetic material that causes the physical features and developmental delays associated with DS.
Down syndrome is a result of a genetic abnormality that is present from the stage of a single fertilized egg. Specifically, it is when the embryo has three copies of chromosome #21 instead of the normal two copies. It is therefore also known as trisomy 21.
This being said, you cannot "get" down syndrome - you are either born with it or without it.
Chromosome 21.
Yes
Down syndrome occurs because of the extra chromosome on chromosome 21. If you go onto google images and type in karyotype of Down syndrome, you will find a picture of the extra chromosome. Instead of having two chromosomes on chromosome 21, there is an extra. Type your answer here...
Down Syndrome is when there is an extra chromosome in someones DNA. More exactly it is when the 21st chromosome has an extra one.
Down Syndrome is caused by a triplication of the 21st chromosome.
47There are 47 chromosomes in someone with Down syndrome; the 21st pair has an extra chromosome. Most people have 46 chromosomes. Down syndrome is also known as "Trisomy 21" - a reference to the fact that someone with Down syndrome has 3 pairs of chromosomes on their 21st pair.
Anyone with an extra chromosome 21.
If someone has an extra chromosome it means there was a genetic mutation that is abnormal in human development. It may result in problems with the person affecting them on a basic level, or may go fully unnoticed. A common disorder that can be caused by having an extra chromosome is Down's Syndrome.
Down Syndrome is known as trisomy 21 because someone with the syndrome has 3 chromosomes of the same type when we are only supposed to have 2 (one from each parent). Chromosomes are paired and numbered so Down Syndrome is the result of having 3 of the #21 chromosome. The body will not know what to do with the extra chromosome so as a precautionary measure it will shut down all 3 and the genes that are within the chromosomes can no longer be accessed. So as you can see, Down Syndrome is not from being inherited by a specific gene. It is due to an error in meiosis in either the mother or the father.
Down Syndrome is caused by extra genetic material on Chromosome 21. About half of the children of people who have Down Syndrome are born with Down Syndrome themselves. See the Related Linksbelow to view an article about the genetics of Down Syndrome.
The causes of a hereditary disease is a missing chromosome, and extra chromosome. Like in Down Syndrome there is an extra chromosome 26.
Angelman syndrome is a genetic disorder, as is Down syndrome. But they are not the same. Angelman Syndrome involves a deletion of Chromosome 15, whereas people with Down syndrome have an extra copy of Chromosome 21.
Down syndrome
Down syndrome is a chromosomal disorder. It is caused by having 1 extra chromosome (chromosome 21).