Question 1

Which clinical feature in a newborn baby girl suggests the possibility of Turner syndrome?

Accepted Answer

A) Absence of Babinski reflex 
B) Presence of a webbed neck 
C) Presence of epicanthal folds 
D) Absence of irises of both eyes 
A) Absence of Babinski reflex 
B) Presence of a webbed neck 
C) Presence of epicanthal folds 
D) Absence of irises of both eyes B

Question 2

Which health screening activity is most important for girls and women with Turner syndrome?

Accepted Answer

A) Mammography 
B) Test for osteoarthritis 
C) Blood pressure screening 
D) Pulmonary function testing 
A) Mammography 
B) Test for osteoarthritis 
C) Blood pressure screening 
D) Pulmonary function testing C

Question 3

What factor most strongly influences the development of the paramesonephric tissue into female sex organs?

Accepted Answer

A) Proper positioning of the bipotential gonad 
B) The presence of estrogen during puberty 
C) The presence of two X chromosomes 
D) The absence of a Y chromosome 
A) Proper positioning of the bipotential gonad 
B) The presence of estrogen during puberty 
C) The presence of two X chromosomes 
D) The absence of a Y chromosome D

Question 4

A male patient is tall and has some gynecomastia along with a low sperm count. During infertility testing, he was found to have a 47,XXY karyotype. Which disorder isconsistent with these findings?

Accepted Answer

A) Normal male 
B) Turner syndrome 
C) Klinefelter syndrome 
D) Testicular feminization syndrome 
A) Normal male 
B) Turner syndrome 
C) Klinefelter syndrome 
D) Testicular feminization syndrome

Question 5

On which chromosome is the androgen receptor (AR) gene located?

Accepted Answer

A) 1 
B) 21 
C) X 
D) Y 
A) 1 
B) 21 
C) X 
D) Y

Question 6

What is the function of the FMR1 gene?

Accepted Answer

A) Promoting brain development and maintaining neuronal synapses 
B) Ensuring the expression of all other genes present on the X chromosome 
C) Preventing amyloid plaque deposits and formation of neuronal tangles in the brain 
D) Maintaining the structural integrity of the histone proteins surrounding the X chromosome 
A) Promoting brain development and maintaining neuronal synapses 
B) Ensuring the expression of all other genes present on the X chromosome 
C) Preventing amyloid plaque deposits and formation of neuronal tangles in the brain 
D) Maintaining the structural integrity of the histone proteins surrounding the X chromosome

Question 7

A man and his sister are both affected with a mitochondrial disorder. Because the sister has two children who also have the disorder, the man is concerned about thepossibility of also having children with the disorder. What is the estimated risk for each pregnancy of this man producing a child with the same mitochondrial disorder that he has if his wife does not have a mitochondrial disorder?

Accepted Answer

A) 100% 
B) 50% 
C) 25% 
D) 0% 
A) 100% 
B) 50% 
C) 25% 
D) 0%

Question 8

Which process can cause a person with an XY genotype to have a female phenotype?

Accepted Answer

A) Pregnancy resulting from artificial insemination in which the semen donor is homosexual 
B) Mating of a man who has Klinefelter syndrome with a woman who has Turner syndrome 
C) An epigenetic disorder in which the X chromosome inactivates the Y chromosome 
D) Failure of gene expression resulting in a complete absence of androgen receptors 
A) Pregnancy resulting from artificial insemination in which the semen donor is homosexual 
B) Mating of a man who has Klinefelter syndrome with a woman who has Turner syndrome 
C) An epigenetic disorder in which the X chromosome inactivates the Y chromosome 
D) Failure of gene expression resulting in a complete absence of androgen receptors

Question 9

What is the most likely mechanism for a 45,X karyotype?

Accepted Answer

A) Anticipation 
B) Nondisjunction 
C) Expansion 
D) Heteroplasmy 
A) Anticipation 
B) Nondisjunction 
C) Expansion 
D) Heteroplasmy

Question 10

Why is the incidence of an extra Y chromosome in the general population unknown?

Accepted Answer

A) The phenotype is that of a normal male. 
B) Most conceptions with 47,XYY are spontaneously aborted. 
C) The life expectancy for males with 47,XYY is often short. 
D) The majority of males with this sex chromosome abnormality are institutionalized. 
A) The phenotype is that of a normal male. 
B) Most conceptions with 47,XYY are spontaneously aborted. 
C) The life expectancy for males with 47,XYY is often short. 
D) The majority of males with this sex chromosome abnormality are institutionalized.

Question 11

What is the risk for a man with a 47,XYY karyotype to produce a child with a 47,XYY karyotype?

Accepted Answer

A) 100% 
B) 50% 
C) 25% 
D) 0% 
A) 100% 
B) 50% 
C) 25% 
D) 0%

Question 12

Which of the following mechanisms in fragile X syndrome (FXS) leads to expression of the disorder?

Accepted Answer

A) Trinucleotide repeat sequences interspersed with the exons of the FMR1 gene, resulting in the production of an abnormal protein 
B) Trinucleotide repeat sequences causing methylation of the FMR1 gene, thus silencing its expression 
C) Increased production of microRNA molecules that interfere with the transcription of the FMR1 gene 
D) Increased production of microRNA molecules that interfere with the translation of the FMR1 gene 
A) Trinucleotide repeat sequences interspersed with the exons of the FMR1 gene, resulting in the production of an abnormal protein 
B) Trinucleotide repeat sequences causing methylation of the FMR1 gene, thus silencing its expression 
C) Increased production of microRNA molecules that interfere with the transcription of the FMR1 gene 
D) Increased production of microRNA molecules that interfere with the translation of the FMR1 gene

Question 13

Which of the following definitions accurately represents the concept of expansion?

Accepted Answer

A) The phenotype of a genetic condition is expressed with greater severity and at earlier ages with succeeding generations. 
B) The number of trinucleotide repeat sequences within the noncoding region of a specific gene allele is increased. 
C) The number of copies of a specific gene allele is amplified on one chromosome of a homologous pair. 
D) A specific gene allele has at least two copies of every exon within the gene. 
A) The phenotype of a genetic condition is expressed with greater severity and at earlier ages with succeeding generations. 
B) The number of trinucleotide repeat sequences within the noncoding region of a specific gene allele is increased. 
C) The number of copies of a specific gene allele is amplified on one chromosome of a homologous pair. 
D) A specific gene allele has at least two copies of every exon within the gene.

Question 14

Which single physical feature is most often associated with a 47,XXX karyotype?

Accepted Answer

A) Infertility 
B) Large breasts 
C) Female-pattern baldness 
D) Height greater than siblings 
A) Infertility 
B) Large breasts 
C) Female-pattern baldness 
D) Height greater than siblings

Question 15

Which trait or characteristic in a 10-year-old-girl would lead her pediatrician to consider the possibility of androgen insensitivity syndrome?

Accepted Answer

A) Her ears are large and stick out. 
B) She is color-blind, and her father is not. 
C) She is an inch taller than her siblings were at age 10. 
D) Her nipples and breasts have not started to change and develop. 
A) Her ears are large and stick out. 
B) She is color-blind, and her father is not. 
C) She is an inch taller than her siblings were at age 10. 
D) Her nipples and breasts have not started to change and develop.

Question 16

Which condition or health problem is more common in women who have an FMR1 mutation?

Accepted Answer

A) Emotional instability with inappropriate expression of anger 
B) Patchy areas of decreased skin pigmentation 
C) Progressive skeletal muscle weakness 
D) Menopause before age 40 years 
A) Emotional instability with inappropriate expression of anger 
B) Patchy areas of decreased skin pigmentation 
C) Progressive skeletal muscle weakness 
D) Menopause before age 40 years

Question 17

Which feature is common among people who have Klinefelter syndrome (47,XXY) or a karyotype with 47,XXX but not among people who have Down syndrome or Edward syndrome?

Accepted Answer

A) Severely reduced cognition 
B) Cleft palate 
C) Tall stature 
D) Infertility 
A) Severely reduced cognition 
B) Cleft palate 
C) Tall stature 
D) Infertility

Question 18

Which type of problem results from mutations in mitochondrial DNA (mtDNA)?

Accepted Answer

A) Reduced cellular energy 
B) Balanced translocations 
C) Excessive "crossing over" 
D) Single-nucleotide polymorphisms 
A) Reduced cellular energy 
B) Balanced translocations 
C) Excessive "crossing over" 
D) Single-nucleotide polymorphisms

Question 19

At what specific location on an X chromosome is a break most likely to occur in fragile X syndrome?

Accepted Answer

A) The centromere 
B) End of the p arm 
C) End of the q arm 
D) Within the nucleosome 
A) The centromere 
B) End of the p arm 
C) End of the q arm 
D) Within the nucleosome

Question 20

What would be the expected consequence to two daughter cells after mitosis if the ability to produce mitochondria was lost?

Accepted Answer

A) Cell commitment and differentiation would fail to occur. 
B) The process of protein synthesis could not be controlled. 
C) The rate and amount of ATP production would be limited. 
D) Future cell division would result in an uneven number of cells. 
A) Cell commitment and differentiation would fail to occur. 
B) The process of protein synthesis could not be controlled. 
C) The rate and amount of ATP production would be limited. 
D) Future cell division would result in an uneven number of cells.

Which clinical feature in a newborn baby girl suggests the possibility of Turner syndrome?

Which health screening activity is most important for girls and women with Turner syndrome?

What factor most strongly influences the development of the paramesonephric tissue into female sex organs?

A male patient is tall and has some gynecomastia along with a low sperm count. During infertility testing, he was found to have a 47,XXY karyotype. Which disorder isconsistent with these findings?

On which chromosome is the androgen receptor (AR) gene located?

What is the function of the FMR1 gene?

Which process can cause a person with an XY genotype to have a female phenotype?

What is the most likely mechanism for a 45,X karyotype?

Why is the incidence of an extra Y chromosome in the general population unknown?

What is the risk for a man with a 47,XYY karyotype to produce a child with a 47,XYY karyotype?

Which of the following mechanisms in fragile X syndrome (FXS) leads to expression of the disorder?

Which of the following definitions accurately represents the concept of expansion?

Which single physical feature is most often associated with a 47,XXX karyotype?

Which trait or characteristic in a 10-year-old-girl would lead her pediatrician to consider the possibility of androgen insensitivity syndrome?

Which condition or health problem is more common in women who have an FMR1 mutation?

Which feature is common among people who have Klinefelter syndrome (47,XXY) or a karyotype with 47,XXX but not among people who have Down syndrome or Edward syndrome?

Which type of problem results from mutations in mitochondrial DNA (mtDNA)?

At what specific location on an X chromosome is a break most likely to occur in fragile X syndrome?

What would be the expected consequence to two daughter cells after mitosis if the ability to produce mitochondria was lost?

DNA Structure and Function

Protein Synthesis

Genetic Influence on Cell Division, Differentiation, and Gametogenesis

Patterns of Inheritance

Epigenetic Influences on Gene Expression

Autosomal Inheritance and Disorders

Family History and Pedigree Construction

Congenital Anomalies, Basic Dysmorphology, and Genetic Assessment

Enzyme and Collagen Disorders

Common Childhood-Onset Genetic Disorders

Common Adult-Onset Disorders

Cardiovascular Disorders

The Genetics of Cancer

Genetic Contributions to Psychiatric and Behavioral Disorders

Genetic and Genomic Testing

Assessing Genomic Variation in Drug Response

Health Professionals and Genomic Care

Financial, Ethical, Legal, and Social Considerations

Genetic and Genomic Variation

Filters

Exam 7: Sex Chromosome and Mitochondrial Inheritance and Disorders

Which clinical feature in a newborn baby girl suggests the possibility of Turner syndrome?

Which health screening activity is most important for girls and women with Turner syndrome?

What factor most strongly influences the development of the paramesonephric tissue into female sex organs?

A male patient is tall and has some gynecomastia along with a low sperm count. During infertility testing, he was found to have a 47,XXY karyotype. Which disorder isconsistent with these findings?

On which chromosome is the androgen receptor (AR) gene located?

What is the function of the FMR1 gene?

Which process can cause a person with an XY genotype to have a female phenotype?

What is the most likely mechanism for a 45,X karyotype?

Why is the incidence of an extra Y chromosome in the general population unknown?

What is the risk for a man with a 47,XYY karyotype to produce a child with a 47,XYY karyotype?

Which of the following mechanisms in fragile X syndrome (FXS) leads to expression of the disorder?

Which of the following definitions accurately represents the concept of expansion?

Which single physical feature is most often associated with a 47,XXX karyotype?

Which trait or characteristic in a 10-year-old-girl would lead her pediatrician to consider the possibility of androgen insensitivity syndrome?

Which condition or health problem is more common in women who have an FMR1 mutation?

Which feature is common among people who have Klinefelter syndrome (47,XXY) or a karyotype with 47,XXX but not among people who have Down syndrome or Edward syndrome?

Which type of problem results from mutations in mitochondrial DNA (mtDNA)?

At what specific location on an X chromosome is a break most likely to occur in fragile X syndrome?

What would be the expected consequence to two daughter cells after mitosis if the ability to produce mitochondria was lost?

DNA Structure and Function

Protein Synthesis

Genetic Influence on Cell Division, Differentiation, and Gametogenesis

Patterns of Inheritance

Epigenetic Influences on Gene Expression

Autosomal Inheritance and Disorders

Family History and Pedigree Construction

Congenital Anomalies, Basic Dysmorphology, and Genetic Assessment

Enzyme and Collagen Disorders

Common Childhood-Onset Genetic Disorders

Common Adult-Onset Disorders

Cardiovascular Disorders

The Genetics of Cancer

Genetic Contributions to Psychiatric and Behavioral Disorders

Genetic and Genomic Testing

Assessing Genomic Variation in Drug Response

Health Professionals and Genomic Care

Financial, Ethical, Legal, and Social Considerations

Genetic and Genomic Variation

Filters