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Some gametes may have an extra copy of some genes.
Meiotic nondisjunction. In meiosis I or II, chromosome pair 21 fail to separate correctly, leaving one gamete with an extra chromosome 21.
Down Syndrom
An XYY zygote can be formed if a pair of sex chromosomes fails to separate during meiosis, so the gamete formed has both the X and Y chromosomes. This gamete would then meet the other gamete from the other cell that would contain a Y sex chromosome. The resulting zygote that is formed would have XYY sex chromosomes. This abnormalty where there is an extra chromosome or is missing a chromosome is called nondisjunction.
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.
an error in meiotic cell division
Addition of a pair of chromosomes to a diploid set results in tetrasomic condition. Tetrasomics may be represented as 2N+2. Tetrasomics may arise when two abonormal gametes produced as a result of non-disjuction unite, with each gamete carrying an extra chromosome of the same pair as shown below. AABBCCDD a diploid cell----meiosis and non disjuction AABC Gamete carrying an extra chromosome--- BC Gamete short of one chromosome. Now if this Gamete (AABC) unites with another gamete of the same kind (AABC), we get tetrasomic AAAABBCC.
It gives one of the gametes an extra chromosome and leaves the other gamete with one less chromosome.
Down's Syndrome is caused due to the presence of an extra 21st chromosome, resulting in 3 sets of 21st chromosome instead of just 2. This is because during Anaphase II of Meiosis II non-disjunction occurs and instead of one 21st chromosome going into each gamete, both go into one of the gametes and none goes into the other. When a normal gamete fuses with the gamete with an extra21st chromosome, it forms a zygote with 3 sets of 21st chromosome instead of 2 and that is known as Down's Syndrome.
two chromosomall diseases that aren't inherited are Downs Syndrome, which is an extra chromosome on the number 21, it occurs in 1 in 650 births, often in women over 35, and Klinefelter's Syndrome, which is the presence of an extra x cromosome, ie XXY, it is a result of nondisjunction during gamete formation.
A trisomy. Trisomies are usually fatal in all chromosome pairs except 5, 13, 21 (these cause Down syndrome), and 23 (The chromosome pair that determines gender)
Some gametes may have an extra copy of some genes.
Meiotic nondisjunction. In meiosis I or II, chromosome pair 21 fail to separate correctly, leaving one gamete with an extra chromosome 21.
Down Syndrom
Babies are born with an extra chromosome.
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.
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...