HEREDITY
MUTATIONS
Question
[CLICK ON ANY CHOICE TO KNOW THE RIGHT ANSWER]
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inversion
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dis-location
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frame shift
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trisomy, such as down syndrome
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Detailed explanation-1: -Nondisjunction causes abnormal number chromosomes in all the cells called aneuploidy or in some cells called mosaicism. Some of the important examples are: Down’s syndrome – Trisomy of autosomes, i.e. chromosome 21. It contains one extra chromosome 21.
Detailed explanation-2: -Trisomy 21 (Nondisjunction) Down syndrome is usually caused by an error in cell division called “nondisjunction.” Nondisjunction results in an embryo with three copies of chromosome 21 instead of the usual two. Prior to or at conception, a pair of 21st chromosomes in either the sperm or the egg fails to separate.
Detailed explanation-3: -Nondisjunction of a single chromosome will produce germ cells that have either two (disomy) or zero (nullisomy) copies of the specific chromosome. If a germ cell with an extra chromosome is combined with a chromosomally normal germ cell, the product will be trisomic (i.e., having 47 chromosomes).
Detailed explanation-4: -In Nondisjunction Trisomy 21, the most typical type of Down syndrome, there is a failure of the chromosome 21 pair to disjoin from each other or divide properly in the egg or sperm cells, leaving an extra number-21 chromosome in each cell. Trisomy 21 accounts for 95% of Down syndrome cases.
Detailed explanation-5: -Trisomy 21 or Down syndrome (DS) is one of the most common chromosomal abnormalities. The majority of full trisomy 21 is caused by chromosomal nondisjunction occurring during maternal meiotic division (∼90%). Errors occur more frequently in the first maternal meiotic division than the second (73% vs.