Chromosomal aberrations refer to structural changes in chromosomes that can include deletions, duplications, inversions, and translocations. A deletion occurs when a portion of a chromosome or DNA sequence is omitted during replication. A duplication happens when a chromosomal segment acquires an extra copy at its original location. An inversion involves a chromosome splitting and the resultant DNA fragment reversing and reinserting in the chromosome. A translocation occurs when a chromosome breaks and the pieces reattach to different chromosomes.
Chromosomal aberrations refer to structural changes in chromosomes that can include deletions, duplications, inversions, and translocations. A deletion occurs when a portion of a chromosome or DNA sequence is omitted during replication. A duplication happens when a chromosomal segment acquires an extra copy at its original location. An inversion involves a chromosome splitting and the resultant DNA fragment reversing and reinserting in the chromosome. A translocation occurs when a chromosome breaks and the pieces reattach to different chromosomes.
Chromosomal aberrations refer to structural changes in chromosomes that can include deletions, duplications, inversions, and translocations. A deletion occurs when a portion of a chromosome or DNA sequence is omitted during replication. A duplication happens when a chromosomal segment acquires an extra copy at its original location. An inversion involves a chromosome splitting and the resultant DNA fragment reversing and reinserting in the chromosome. A translocation occurs when a chromosome breaks and the pieces reattach to different chromosomes.
1.Compare and contrast the different chromosomal aberrations.
Chromosomal Aberrations.
Deletion A deletion in genetics is a
mutation (a genetic aberration) in which a portion of a chromosome or a DNA sequence is omitted during DNA replication. Deletions are also known as gene deletions, deficiencies, or deletion mutations (sign: ). A base or an entire chromosome can have any number of nucleotides removed from it.
Duplication A chromosomal segment
acquires a copy at its original place on the chromosome, which results in a duplication. Duplications can be made in the original (direct) direction or inverted orientation. Other structural chromosomal defects don't cause any genetic material to be gained or lost. Inversion Inversions. When a chromosome splits in two, the resultant fragment of DNA is reversed and reinserted into the chromosome, causing an inversion. The chromosomal breaks may or may not result in the loss of genetic material.
Translocation A translocation, as related
to genetics, occurs when a chromosome breaks and the (typically two) fragmented pieces re-attach to different chromosomes. The detection of chromosomal translocations can be important for the diagnosis of certain genetic diseases and disorders.
2.Can you prevent chromosomal aberration? Explain our answer.
- By taking care of their own dietary requirements, minimizing exposure to risky drugs, and seeing a doctor before getting pregnant, parents can lessen the chance of chromosomal abnormalities in their children. Healthy eating, quitting smoking and drinking alcohol, and taking prenatal vitamins before getting pregnant are all examples of general risk reduction techniques. Pregnancies with a mother above the age of 35 are more likely to result in chromosomal abnormalities. A healthcare professional could suggest genetic counseling to go through alternatives, including assisted reproductive technologies, if a chromosomal issue has been found in the family. 3.Is chromosomal aberration a valid excuse for abortion? - Abortion is a possibility for people for a variety of reasons, including when a problem is found during prenatal testing. If your baby has a chromosomal problem as determined by an ultrasound or other tests, you may be thinking about your choices, including ending the pregnancy.