Individuals with Down syndrome are more numerous then individuals with an extra chromosome 3 or 16 because the those conditions are much more likely to be fatal (resulting in miscarriage or other early deaths).
trisomy There several types of trisomy, the most well known is probably Down syndrome, which is trisomy 21.
Well down syndrome is causes by the 21st chromosome of a sex cell doubling, and so once fertilisation with the egg commences there will be 3 21st chromosomes. When you have 45 their is multiple things that can happen, the only consistent one is Turner Syndrome, which basically stunts puberty. This only happens in females and it is when they have X instead of XX.
No " following, but a condition such as trisomy 21, Downs syndrome, is caused by nondisjuction. The chromosomes fail to separate properly and one child is left with an extra chromosome number 21. The potetial other children that could have been born of this nondijuction event, those with only one chromosome 21, are not viable.
Nondisjunction is the failure of a homolog to separate during meiosis causing trisomy (an extra chromosome) or monosomy (a missing chromosome), it can be harmful because it is a mutation that can cause many devastating disease, for example nondisjunction of the 21st chromosome causes down syndrome, another example of nondisjunction being harmful, is nondisjunction of the sex chromosomes, causing Turner's or Klinefelter's syndrome two very devastating diseases.
Down syndrome results from a nondisjunction during cell division. That is, homologous chromosomes 21 fail to separate in meiosis I, or sister chromatids 21 during meiosis II or mitosis. Down syndrome is caused by trisomy of chromosome 21 (an extra chromosome to the usual two), which is an autosomal chromosome. Therefore it is not a sex linked disorder.
The extra chromosome 13 causes numerous physical and mental abnormalities, especially heart defects.
The causes of a hereditary disease is a missing chromosome, and extra chromosome. Like in Down Syndrome there is an extra chromosome 26.
deletion syndrome is a disorder caused by the deletion of a small piece of chromosome 22. The deletion occurs near the middle of the chromosome at a location designated q11.2.
Down syndrome is caused by the presence of a third chromosome 21
An extra copy of Chromosome 18
Down syndrome is neither caused by dominant or recessive chromosomes it is simply caused by an error in the translation process of chromosome 21.
Down's syndrome is caused by trisomy of the 21st chromosome. This is mostly caused when the chromosome pair fails to separate properly (nondisjunction).
Having an extra copy of chromosome 21. You are supposed to have 2; when you have 3 (trisomy 21), Down's Syndrome is the result.
3 Pairs of Chromosome 21There are 47 chromosomes in someone with Down syndrome (most people have 46); the 21st pair has an extra chromosome. Down syndrome is also known as "Trisomy 21" - a reference to the fact that someone with Down syndrome has 3 pairs of chromosomes 21.
Mutations in the iduronate-2-sulphatase (IDS) gene cause both forms of MPS II (mild and severe). Nearly all individuals with Hunter syndrome are male, because the gene that causes the condition is located on the X chromosome.
Down Syndrome is a the addition of an extra chromosome and not really related to evolution. It is more of a genetic mutation that causes this event to occur.
A partial trisomy or tetrasomy of the top part of chromosome 22 in proximal 22q11