Question Video: Identifying Which Person or Couple Are Most Likely to be Offered Genetic Screening | Nagwa Question Video: Identifying Which Person or Couple Are Most Likely to be Offered Genetic Screening | Nagwa

Question Video: Identifying Which Person or Couple Are Most Likely to be Offered Genetic Screening Biology • First Year of Secondary School

All of the individuals described below are planning on having children in the near future. Person A has a grandparent who is an identical twin. Person B has a family history of thalassemia, a disorder affecting the hemoglobin of the blood. Person C lives in a small community and is marrying their first cousin. Person D already has two girls and would like a boy. Which of the people listed above would most likely be offered genetic screening?

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Video Transcript

All of the individuals described below are planning on having children in the near future. Person A has a grandparent who is an identical twin. Person B has a family history of thalassemia, a disorder affecting the hemoglobin of the blood. Person C lives in a small community and is marrying their first cousin. And person D already has two girls and would like a boy. Which of the people listed above would most likely be offered genetic screening?

Genetic screening is the process by which a person’s DNA is studied to identify any genes that could cause a genetic disorder. It is commonly offered to those with a family history of a specific illness or disease. Genetic screening can be carried out either before a couple tries to conceive or during pregnancy. For high-risk parents or those that are related, these tests are offered in the prepregnancy stage. One type of genetic screening is called carrier screening. This is used for people with a history of a genetic disease but who do not have symptoms. So it is unclear if they carry the allele for that disease. We can see that this description applies to one of our options. Person B has a family history of thalassemia.

Genetic screening may also be offered to those that live in isolated communities or communities that have a history of a particular genetic disorder. This is because, typically, these communities are made up of family groups and individuals are highly related. This means that if this grandparent was a carrier for a recessive genetic disease like Tay–Sachs, they could pass this on to their children. Their children, shown here, are now carriers for the disease. But they could pass the allele on to their own children. If these two individuals who are cousins were now to have their own children, they have a much higher risk of passing on two recessive alleles to their children. This means that their offspring are much more likely to inherit Tay–Sachs disease. This means that genetic testing is likely to be offered to another one of our individuals, person C, who lives in a small community and is marrying their first cousin.

Genetic screening is only offered to those who are at risk of passing on genetic diseases to their offspring. This helps prevent the spread of disease and allows parents to prepare themselves mentally, physically, and financially for having a child with a genetic disorder. It is not offered to people who would like to choose the sex of their child, so we can exclude person D. And we can also exclude person A, as genetic screening will not be offered to people who are expecting or who would like twins.

So the correct answer to which people would be offered genetic screening is person B and person C.

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