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.
No, trisomy is caused by an error in meiosis, not a mutation.
Trisomy is when you have 3 of one chromosome, it is most commonly seen on Chromosome 21. It is usually caused by non-disjunction of the chromosomes during meiosis
Gametes
during meiosis
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
during meiosis
Trisomy 18 can be detected before birth
Gametes
during meiosis
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).
Very sure that it is insertion, because there are three chromosome 18s instead of two.
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
Down's Syndrome Kleinfelter's Syndrome
during meiosis
trisomy
There is no cure for trisomy 18
Trisomy an abnormality in chromosomal development.
Downs syndrome is caused by a genetic mutation called trisomy. Trisomy is when an extra chromosome is present on one set of chromosomes, so instead of the 46 chromosomes of a normal human there are 47. Trisomy can often result in miscarriage as the body cannot cope well with extra chromosomes. Downs syndrome is when there is an extra chromosome 21. Other genetic defects which are caused by trisomy are Edwards syndrome and Patau syndrome.
Down's syndrome is caused by trisomy of the 21st chromosome. This is mostly caused when the chromosome pair fails to separate properly (nondisjunction).