A human female with Turner syndrome (47, X) also expresses the X-linked trait hemophilia, as did her father. Which of her parents underwent nondisjunction during meiosis, giving rise to the gamete responsible for the syndrome?

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Answer 1

Textbook Question

Chapter 8, Problem 1NST

A human female with Turner syndrome (47, X) also expresses the X-linked trait hemophilia, as did her father. Which of her parents underwent nondisjunction during meiosis, giving rise to the gamete responsible for the syndrome?

Expert Solution & Answer

Summary Introduction

To determine: The parent whose genome has undergone nondisjunction during meiosis that resulted in a human female with Turner syndrome (47, X) along with X-linked trait hemophilia.

Introduction: Turner syndrome is a condition in which female which is born have only 45 chromosomes and the missing chromosome is an X-chromosome. Since the X chromosome is missing the various proteins which are coded by the X-chromosome are affected. Thy symptoms of turner syndrome include short stature, reproductive sterility, visual impairments, nonverbal learning disability and various other conditions.

Explanation of Solution

Aneuploidy is a condition in which a person loses only one chromosome but the other complementary chromosome is present. In non-disjunction the chromosomes are unable to separate the linked homologs or chromatids during mitosis or meiosis.

Hemophilia is an X-linked trait and since the father and daughter both are suffering from this condition, this implies that the X chromosome from the father was inherited to the girl. So, it can be concluded that the Turner’s syndrome arises due to non-disjunction observed in the mother, which prevents the entry of X-chromosome from the mother resulting in only a single X-chromosome that has been inherited from the father.

Conclusion

The Turner syndrome is a result of nondisjunction of the chromosomes during the formation of gamete in mother.

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Answer 2

Textbook Question

Chapter 8, Problem 1NST

A human female with Turner syndrome (47, X) also expresses the X-linked trait hemophilia, as did her father. Which of her parents underwent nondisjunction during meiosis, giving rise to the gamete responsible for the syndrome?

Expert Solution & Answer

Summary Introduction

To determine: The parent whose genome has undergone nondisjunction during meiosis that resulted in a human female with Turner syndrome (47, X) along with X-linked trait hemophilia.

Introduction: Turner syndrome is a condition in which female which is born have only 45 chromosomes and the missing chromosome is an X-chromosome. Since the X chromosome is missing the various proteins which are coded by the X-chromosome are affected. Thy symptoms of turner syndrome include short stature, reproductive sterility, visual impairments, nonverbal learning disability and various other conditions.

Explanation of Solution

Aneuploidy is a condition in which a person loses only one chromosome but the other complementary chromosome is present. In non-disjunction the chromosomes are unable to separate the linked homologs or chromatids during mitosis or meiosis.

Hemophilia is an X-linked trait and since the father and daughter both are suffering from this condition, this implies that the X chromosome from the father was inherited to the girl. So, it can be concluded that the Turner’s syndrome arises due to non-disjunction observed in the mother, which prevents the entry of X-chromosome from the mother resulting in only a single X-chromosome that has been inherited from the father.

Conclusion

The Turner syndrome is a result of nondisjunction of the chromosomes during the formation of gamete in mother.

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Answer 3

Textbook Question

Chapter 8, Problem 1NST

A human female with Turner syndrome (47, X) also expresses the X-linked trait hemophilia, as did her father. Which of her parents underwent nondisjunction during meiosis, giving rise to the gamete responsible for the syndrome?

Expert Solution & Answer

Summary Introduction

To determine: The parent whose genome has undergone nondisjunction during meiosis that resulted in a human female with Turner syndrome (47, X) along with X-linked trait hemophilia.

Introduction: Turner syndrome is a condition in which female which is born have only 45 chromosomes and the missing chromosome is an X-chromosome. Since the X chromosome is missing the various proteins which are coded by the X-chromosome are affected. Thy symptoms of turner syndrome include short stature, reproductive sterility, visual impairments, nonverbal learning disability and various other conditions.

Explanation of Solution

Aneuploidy is a condition in which a person loses only one chromosome but the other complementary chromosome is present. In non-disjunction the chromosomes are unable to separate the linked homologs or chromatids during mitosis or meiosis.

Hemophilia is an X-linked trait and since the father and daughter both are suffering from this condition, this implies that the X chromosome from the father was inherited to the girl. So, it can be concluded that the Turner’s syndrome arises due to non-disjunction observed in the mother, which prevents the entry of X-chromosome from the mother resulting in only a single X-chromosome that has been inherited from the father.

Conclusion

The Turner syndrome is a result of nondisjunction of the chromosomes during the formation of gamete in mother.

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Subscribe now to access step-by-step solutions to millions of textbook problems written by subject matter experts!

Answer 4

Textbook Question

Chapter 8, Problem 1NST

A human female with Turner syndrome (47, X) also expresses the X-linked trait hemophilia, as did her father. Which of her parents underwent nondisjunction during meiosis, giving rise to the gamete responsible for the syndrome?

Expert Solution & Answer

Summary Introduction

To determine: The parent whose genome has undergone nondisjunction during meiosis that resulted in a human female with Turner syndrome (47, X) along with X-linked trait hemophilia.

Introduction: Turner syndrome is a condition in which female which is born have only 45 chromosomes and the missing chromosome is an X-chromosome. Since the X chromosome is missing the various proteins which are coded by the X-chromosome are affected. Thy symptoms of turner syndrome include short stature, reproductive sterility, visual impairments, nonverbal learning disability and various other conditions.

Explanation of Solution

Aneuploidy is a condition in which a person loses only one chromosome but the other complementary chromosome is present. In non-disjunction the chromosomes are unable to separate the linked homologs or chromatids during mitosis or meiosis.

Hemophilia is an X-linked trait and since the father and daughter both are suffering from this condition, this implies that the X chromosome from the father was inherited to the girl. So, it can be concluded that the Turner’s syndrome arises due to non-disjunction observed in the mother, which prevents the entry of X-chromosome from the mother resulting in only a single X-chromosome that has been inherited from the father.

Conclusion

The Turner syndrome is a result of nondisjunction of the chromosomes during the formation of gamete in mother.

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Subscribe now to access step-by-step solutions to millions of textbook problems written by subject matter experts!

Answer 5

Textbook Question

Answer 6

Textbook Question

Answer 7

Expert Solution & Answer

Summary Introduction

To determine: The parent whose genome has undergone nondisjunction during meiosis that resulted in a human female with Turner syndrome (47, X) along with X-linked trait hemophilia.

Introduction: Turner syndrome is a condition in which female which is born have only 45 chromosomes and the missing chromosome is an X-chromosome. Since the X chromosome is missing the various proteins which are coded by the X-chromosome are affected. Thy symptoms of turner syndrome include short stature, reproductive sterility, visual impairments, nonverbal learning disability and various other conditions.

Explanation of Solution

Aneuploidy is a condition in which a person loses only one chromosome but the other complementary chromosome is present. In non-disjunction the chromosomes are unable to separate the linked homologs or chromatids during mitosis or meiosis.

Hemophilia is an X-linked trait and since the father and daughter both are suffering from this condition, this implies that the X chromosome from the father was inherited to the girl. So, it can be concluded that the Turner’s syndrome arises due to non-disjunction observed in the mother, which prevents the entry of X-chromosome from the mother resulting in only a single X-chromosome that has been inherited from the father.

Conclusion

The Turner syndrome is a result of nondisjunction of the chromosomes during the formation of gamete in mother.

Answer 8

Expert Solution & Answer

Summary Introduction

To determine: The parent whose genome has undergone nondisjunction during meiosis that resulted in a human female with Turner syndrome (47, X) along with X-linked trait hemophilia.

Introduction: Turner syndrome is a condition in which female which is born have only 45 chromosomes and the missing chromosome is an X-chromosome. Since the X chromosome is missing the various proteins which are coded by the X-chromosome are affected. Thy symptoms of turner syndrome include short stature, reproductive sterility, visual impairments, nonverbal learning disability and various other conditions.

Explanation of Solution

Aneuploidy is a condition in which a person loses only one chromosome but the other complementary chromosome is present. In non-disjunction the chromosomes are unable to separate the linked homologs or chromatids during mitosis or meiosis.

Hemophilia is an X-linked trait and since the father and daughter both are suffering from this condition, this implies that the X chromosome from the father was inherited to the girl. So, it can be concluded that the Turner’s syndrome arises due to non-disjunction observed in the mother, which prevents the entry of X-chromosome from the mother resulting in only a single X-chromosome that has been inherited from the father.

Conclusion

The Turner syndrome is a result of nondisjunction of the chromosomes during the formation of gamete in mother.

Answer 9

Expert Solution & Answer

Answer 10

Expert Solution & Answer

Answer 11

Summary Introduction

To determine: The parent whose genome has undergone nondisjunction during meiosis that resulted in a human female with Turner syndrome (47, X) along with X-linked trait hemophilia.

Introduction: Turner syndrome is a condition in which female which is born have only 45 chromosomes and the missing chromosome is an X-chromosome. Since the X chromosome is missing the various proteins which are coded by the X-chromosome are affected. Thy symptoms of turner syndrome include short stature, reproductive sterility, visual impairments, nonverbal learning disability and various other conditions.

Answer 12

Explanation of Solution

Aneuploidy is a condition in which a person loses only one chromosome but the other complementary chromosome is present. In non-disjunction the chromosomes are unable to separate the linked homologs or chromatids during mitosis or meiosis.

Hemophilia is an X-linked trait and since the father and daughter both are suffering from this condition, this implies that the X chromosome from the father was inherited to the girl. So, it can be concluded that the Turner’s syndrome arises due to non-disjunction observed in the mother, which prevents the entry of X-chromosome from the mother resulting in only a single X-chromosome that has been inherited from the father.