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MENDELIAN MODE
OF INHERITANCE AND PEDIGREE ANALYSIS
1. Dent disease is a rare disorder of the kidney in which there is impaired reabsorption of filtered
solutes and progressive renal failure. The following pedigree shows the pattern of inheritance for
this disorder.
b. From your answer to part a, give the most likely genotypes for the
following persons in the pedigree:
I-1: Aa
II- 5: Aa
III- 1: Aa
IV- 2: Aa
I-2: aa
II- 8: aa
III- 3: aa
IV- 1: aa
2. The following pedigree illustrates the inheritance of Duchenne Muscular Dystrophy, a condition
characterized by progressive weakness and degeneration of skeletal muscles due to absence of
dystrophin.
a. On the basis of this pedigree, what do you think is the most likely mode of
inheritance for Duchenne Muscular Dystrophy? Y-linked trait
b. If couple III-7 and III-8 have another child, what is the probability that the
child will have Duchenne Muscular Dystrophy? 25%
c. If III-2 and III-7 mated, what is the probability that one of their children
would have the disease? 50%
a. Assuming the shaded individuals have an autosomal recessive trait, count the
individuals with:
● homozygous genotype: 7
● heterozygous genotype: 4
● unknown genotype: 4
b. What is the most likely mode of inheritance for color blindness in Rod’s family?
c. If Rod marries a woman who has no family history of color blindness, what is the probability that
their first child will be a colorblind male?