Tay-Sachs disease (TSD) is an inborn error of metabolism that
results in death, often in early
childhood. A phenotypically normal couple is considering
having a child. The male had a female
first cousin on his father’s side that died from TSD. The
female had a maternal uncle with TSD.
There are no other known cases in either of the families and
none of the matings has been
between related individuals. Assume this trait is very
rare.
a. Draw a pedigree showing the relevant individuals. Using
defined symbols, show the
genotypes of the relevant individuals.
b. Calculate the probability that the male and female in
question are carriers for TSD.
c. What is the probability that neither of them is a
carrier?
d. What is the probability that one of them is a carrier and
the other is not?