When a genetic disease is present in a family, knowledge of gene transmission patterns can be used to calculate the probability of prospective parents' having affected offspring.A married couple finds out that each had an uncle with Tay-Sachs disease. The question is whether or not the man and woman are heterozygotes as they do not have the disease. If both are heterozygotes or carriers then there is a risk of having an affected child. The pedigree looks like this:
Pedigree can be found here: https://www.ncbi.nlm.nih.gov/books/NBK21257/
What is the probability that their first child will have Tay-Sachs (AR)? (show work)
What is the probability that their second child will have Fanconi Anemia?
What is the risk of an affected child if one of the parents is a carrier?
When a genetic disease is present in a family, knowledge of gene transmission patterns can be used to calculate the probability of prospective parents' having affected offspring.A married couple finds out that each had an uncle with Tay-Sachs disease. The question is whether or not the man and woman are heterozygotes as they do not have the disease. If both are heterozygotes or carriers then there is a risk of having an affected child. The pedigree looks like this:
Pedigree can be found here: https://www.ncbi.nlm.nih.gov/books/NBK21257/
What is the probability that their first child will have Tay-Sachs (AR)? (show work)
What is the probability that their second child will have Fanconi Anemia?
What is the risk of an affected child if one of the parents is a carrier?