The pedigree for the given condition. Introduction: Galactosemia is a limited genetic metabolic disease that influences the capacity of an individual to metabolize the sugar galactose accurately.

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Answer 1

Question

Chapter 2, Problem 70P

A.

Summary Introduction

To determine: The pedigree for the given condition.

Introduction: Galactosemia is a limited genetic metabolic disease that influences the capacity of an individual to metabolize the sugar galactose accurately.

B.

Summary Introduction

To determine: The probability that this child will have galactosemia.

Introduction: Galactosemia is an autosomal recessive disease. An autosomal illness is a condition that does not depends on the sex chromosomes. If two people who possess galactosemia have children, all of them will have galactosemia.

C.

Summary Introduction

To determine: If the first child has galactosemia, the probability that a second child will also be having the same condition.

Introduction: An autosomal recessive disorder indicates both copies of the gene in every cell need to hold the mutation for a person to exhibit indications. The parents of an affected person typically bear one copy of the abnormal gene, though they do not show symptoms of galactosemia.

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Salim and Sara are contemplating having children, but Salim’s brother has galactosemia and Sara’s great-grandmother also had galactosemia. Sara has a sister who has three children, none of whom is affected.a. Construct a genetic pedigree for this family showing the possible genotype of each member.b. What is the probability that Salim and Sara’s first child will have galactosemia? Explain your calculations.

a. The pedigree follows the inheritance of a relatively common trait. Is the trait most likely autosomal dominant, autosomal recessive, X-linked dominant, or X-linked recessive? Explain your reasoning. b. If the couple marked with a “*” had another child, what is the probability that it would be an affected daughter? (Note: this is a compound outcome.)

Pompe disease is a glycogen storage disorder caused by a lack of ⍺-glucosidase, the enzyme that converts glycogen to glucose in the muscles. Babies born with this disorder die by the age of two. pope disease is a genetic disorder caused by the presence of two recessive autosomal alleles. A. A man and a woman heterozygous for the condition have two female unaffected children. Determine, using a Punnett square, the probability, expressed as a whole number percentage, of a fourth baby being born a male with Pompe disease. B. Iftheman,fromthepreviousquestion,hadtypeAbloodandthewomanhadtypeO blood, what would be probability of them having a daughter with type O blood and affected with Pompe disease? (Show clearly your calculations and express your answer as a frequency between 0 - 1 and rounded to 2 decimal places)

Answer 2

Question

Chapter 2, Problem 70P

A.

Summary Introduction

To determine: The pedigree for the given condition.

Introduction: Galactosemia is a limited genetic metabolic disease that influences the capacity of an individual to metabolize the sugar galactose accurately.

B.

Summary Introduction

To determine: The probability that this child will have galactosemia.

Introduction: Galactosemia is an autosomal recessive disease. An autosomal illness is a condition that does not depends on the sex chromosomes. If two people who possess galactosemia have children, all of them will have galactosemia.

C.

Summary Introduction

To determine: If the first child has galactosemia, the probability that a second child will also be having the same condition.

Introduction: An autosomal recessive disorder indicates both copies of the gene in every cell need to hold the mutation for a person to exhibit indications. The parents of an affected person typically bear one copy of the abnormal gene, though they do not show symptoms of galactosemia.

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Answer 3

Question

Chapter 2, Problem 70P

A.

Summary Introduction

To determine: The pedigree for the given condition.

Introduction: Galactosemia is a limited genetic metabolic disease that influences the capacity of an individual to metabolize the sugar galactose accurately.

B.

Summary Introduction

To determine: The probability that this child will have galactosemia.

Introduction: Galactosemia is an autosomal recessive disease. An autosomal illness is a condition that does not depends on the sex chromosomes. If two people who possess galactosemia have children, all of them will have galactosemia.

C.

Summary Introduction

To determine: If the first child has galactosemia, the probability that a second child will also be having the same condition.

Introduction: An autosomal recessive disorder indicates both copies of the gene in every cell need to hold the mutation for a person to exhibit indications. The parents of an affected person typically bear one copy of the abnormal gene, though they do not show symptoms of galactosemia.

Expert Solution & Answer

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Answer 4

Question

Chapter 2, Problem 70P

A.

Summary Introduction

To determine: The pedigree for the given condition.

Introduction: Galactosemia is a limited genetic metabolic disease that influences the capacity of an individual to metabolize the sugar galactose accurately.

B.

Summary Introduction

To determine: The probability that this child will have galactosemia.

Introduction: Galactosemia is an autosomal recessive disease. An autosomal illness is a condition that does not depends on the sex chromosomes. If two people who possess galactosemia have children, all of them will have galactosemia.

C.

Summary Introduction

To determine: If the first child has galactosemia, the probability that a second child will also be having the same condition.

Introduction: An autosomal recessive disorder indicates both copies of the gene in every cell need to hold the mutation for a person to exhibit indications. The parents of an affected person typically bear one copy of the abnormal gene, though they do not show symptoms of galactosemia.

Expert Solution & Answer

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Answer 5

Chapter 2, Problem 70P

A.

Summary Introduction

To determine: The pedigree for the given condition.

Introduction: Galactosemia is a limited genetic metabolic disease that influences the capacity of an individual to metabolize the sugar galactose accurately.

B.

Summary Introduction

To determine: The probability that this child will have galactosemia.

Introduction: Galactosemia is an autosomal recessive disease. An autosomal illness is a condition that does not depends on the sex chromosomes. If two people who possess galactosemia have children, all of them will have galactosemia.

C.

Summary Introduction

To determine: If the first child has galactosemia, the probability that a second child will also be having the same condition.

Introduction: An autosomal recessive disorder indicates both copies of the gene in every cell need to hold the mutation for a person to exhibit indications. The parents of an affected person typically bear one copy of the abnormal gene, though they do not show symptoms of galactosemia.

Answer 6

Chapter 2, Problem 70P

A.

Summary Introduction

To determine: The pedigree for the given condition.

Introduction: Galactosemia is a limited genetic metabolic disease that influences the capacity of an individual to metabolize the sugar galactose accurately.

Answer 7

Chapter 2, Problem 70P

A.

Summary Introduction

To determine: The pedigree for the given condition.

Introduction: Galactosemia is a limited genetic metabolic disease that influences the capacity of an individual to metabolize the sugar galactose accurately.

Answer 8

B.

Summary Introduction

To determine: The probability that this child will have galactosemia.

Introduction: Galactosemia is an autosomal recessive disease. An autosomal illness is a condition that does not depends on the sex chromosomes. If two people who possess galactosemia have children, all of them will have galactosemia.

Answer 9

B.

Summary Introduction

To determine: The probability that this child will have galactosemia.

Introduction: Galactosemia is an autosomal recessive disease. An autosomal illness is a condition that does not depends on the sex chromosomes. If two people who possess galactosemia have children, all of them will have galactosemia.

Answer 10

C.

Summary Introduction

To determine: If the first child has galactosemia, the probability that a second child will also be having the same condition.

Introduction: An autosomal recessive disorder indicates both copies of the gene in every cell need to hold the mutation for a person to exhibit indications. The parents of an affected person typically bear one copy of the abnormal gene, though they do not show symptoms of galactosemia.

Answer 11

C.

Summary Introduction

To determine: If the first child has galactosemia, the probability that a second child will also be having the same condition.

Introduction: An autosomal recessive disorder indicates both copies of the gene in every cell need to hold the mutation for a person to exhibit indications. The parents of an affected person typically bear one copy of the abnormal gene, though they do not show symptoms of galactosemia.

Answer 12

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Answer 13

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Answer 15

Ch. 2 - Prob. 1P Ch. 2 - Prob. 2P Ch. 2 - Prob. 3P Ch. 2 - Prob. 4P Ch. 2 - Prob. 6P Ch. 2 - Prob. 7P Ch. 2 - Prob. 8P Ch. 2 - Prob. 9P Ch. 2 - Prob. 10P Ch. 2 - Prob. 11P

The pedigree for the given condition. Introduction: Galactosemia is a limited genetic metabolic disease that influences the capacity of an individual to metabolize the sugar galactose accurately.

Solution Summary: The author explains that galactosemia is an autosomal recessive form of inheritance that affects the ability of an individual to metabolize the sugar.

Concept explainers

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To determine: The pedigree for the given condition.

Introduction: Galactosemia is a limited genetic metabolic disease that influences the capacity of an individual to metabolize the sugar galactose accurately.

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Chapter 2 Solutions

The pedigree for the given condition. Introduction: Galactosemia is a limited genetic metabolic disease that influences the capacity of an individual to metabolize the sugar galactose accurately.

Solution Summary: The author explains that galactosemia is an autosomal recessive form of inheritance that affects the ability of an individual to metabolize the sugar.

Concept explainers

Videos

To determine: The pedigree for the given condition. Introduction: Galactosemia is a limited genetic metabolic disease that influences the capacity of an individual to metabolize the sugar galactose accurately.

Want to see the full answer?

Chapter 2 Solutions

To determine: The pedigree for the given condition.

Introduction: Galactosemia is a limited genetic metabolic disease that influences the capacity of an individual to metabolize the sugar galactose accurately.