Tay-Sachs disease is a rare human disease in which toxic substances accumulate in nerve cells. The recessive allele responsible for the disease is inherited in a simple Mendelian manner. For unknown reasons, the allele is more common in populations of Ashkenazi Jews of eastern Europe. A woman is planning to marry her first cousin, but the couple discovers that their shared grandfather’s sister died in infancy of Tay-Sachs disease. a. Draw the relevant parts of the pedigree, and show all the genotypes as completely as possible. b. What is the probability that the cousins’ first child will have Tay-Sachs disease, assuming that all people who marry into the family are homozygous normal?

Human Heredity: Principles and Issues (MindTap Course List)
11th Edition
ISBN:9781305251052
Author:Michael Cummings
Publisher:Michael Cummings
Chapter11: Genome Alterations: Mutation And Epigenetics
Section: Chapter Questions
Problem 16QP: Familial retinoblastoma, a rare autosomal dominant defect, arose in a large family that had no prior...
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Tay-Sachs disease is a rare human disease in which toxic substances accumulate in nerve cells. The recessive
allele responsible for the disease is inherited in a simple
Mendelian manner. For unknown reasons, the allele is
more common in populations of Ashkenazi Jews of
eastern Europe. A woman is planning to marry her first
cousin, but the couple discovers that their shared
grandfather’s sister died in infancy of Tay-Sachs
disease.
a. Draw the relevant parts of the pedigree, and show
all the genotypes as completely as possible.
b. What is the probability that the cousins’ first child
will have Tay-Sachs disease, assuming that all people
who marry into the family are homozygous normal?

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