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A trisomy is when a person has 3 versions of a chromosome. 'Normal' humans will only have 2 of each chromosome.
For example, having 3 versions of chromosome 21 is known as Trisomy 21 or Down syndrome.
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If child is born with trisomy when did the mutation occur?
during meiosis
When a child has Trisomy when does the mutation occur?
during meiosis
What are mutation that result in death?
These are called fatal genetic mutations. Same examples are: Tay-Sachs disease, Neimann-Pick disease, Trisomy 18 and Trisomy 13 are "Edwards Syndrome" and "Patau Syndrome," respectively and Cystic fibrosis
When is chill is born with trisomy when did the mutation occur?
Trisomy occurs when there is an extra chromosome present in the cells, typically due to an error in cell division during the formation of sperm or egg cells. This mutation can happen during meiosis, the process of cell division that produces gametes, leading to a fertilized egg with three copies of a chromosome instead of the usual two. In the case of Down syndrome (trisomy 21), for example, this error occurs during the formation of the egg or sperm, and the exact timing can vary, but it generally happens before conception.
What chromosomal mutation causes an extra copy of chromosome 13?
Trisomy 13, also known as Patau syndrome, is a chromosomal mutation where there is an extra copy of chromosome 13 in each cell. This condition can lead to various physical and intellectual disabilities.
If child is born with trisomy when did the mutation occur?
during meiosis
When a child has Trisomy when does the mutation occur?
during meiosis
Trisomy is a mutation that results in a cell having an extra?
A trisomy is a condition in which a person has three copies of a chromosome instead of the usual two copies. A person can have full trisomy (three copies in every cell) or mosaic trisomy (three copies in some cells but not all).
What are mutation that result in death?
These are called fatal genetic mutations. Same examples are: Tay-Sachs disease, Neimann-Pick disease, Trisomy 18 and Trisomy 13 are "Edwards Syndrome" and "Patau Syndrome," respectively and Cystic fibrosis
Type of mutation that causes Trisomy 18?
Trisomy 18 is caused by a type of mutation called nondisjunction, where an error in cell division results in an extra copy of chromosome 18. This leads to the presence of three copies of chromosome 18 in each cell instead of the normal two copies.
When is chill is born with trisomy when did the mutation occur?
Trisomy occurs when there is an extra chromosome present in the cells, typically due to an error in cell division during the formation of sperm or egg cells. This mutation can happen during meiosis, the process of cell division that produces gametes, leading to a fertilized egg with three copies of a chromosome instead of the usual two. In the case of Down syndrome (trisomy 21), for example, this error occurs during the formation of the egg or sperm, and the exact timing can vary, but it generally happens before conception.
What chromosomal mutation causes an extra copy of chromosome 13?
Trisomy 13, also known as Patau syndrome, is a chromosomal mutation where there is an extra copy of chromosome 13 in each cell. This condition can lead to various physical and intellectual disabilities.
What are examples of diseases caused by chromosomal mutation?
Down's Syndrome Kleinfelter's Syndrome
Is color blindness monosomy or trisomy?
trisomy
Can trisomy 18 be cured?
There is no cure for trisomy 18
Trisomy-21 results from a mutation to the chromosomes in?
Trisomy-21, also known as Down syndrome, results from an extra copy of chromosome 21. Instead of the usual two copies, individuals with Down syndrome have three copies of chromosome 21. This extra genetic material can lead to various physical and cognitive differences.
What type of condition is trisomy?
Trisomy an abnormality in chromosomal development.
