Deck 13: Genetic Counseling

Question 1

Inversions are chromosomal mutations that

A) always result in a syndrome.
B) neither increase nor decrease the amount of genetic material in the cell.
C) rarely cause deletions or duplications during gamete formation when crossing-over occurs.
D) result from duplication of a portion of a chromosome.
E) never disrupt gene regulation or cause physical abnormalities.

Answer 1

B

Question 2

When a chromosome carrying an inversion undergoes crossing-over

A) all four chromatids of the tetrad will contain a duplication or deletion.
B) two chromatids will carry both a duplication and a deletion, one will contain the inversion, and one will be normal.
C) two chromatids will carry both a duplication and a deletion, and the other two will contain the inversion.
D) all four chromatids will be normal.
E) two chromatids will carry the inversion, and the other two will be normal.

Answer 2

B

Question 3

Which of the following syndromes is caused by a translocation?

A) Alagille syndrome
B) invdup 15 syndrome
C) Williams syndrome
D) Cri-du-chat syndrome
E) Turner syndrome

Answer 3

A

Question 4

A parent has a deletion on one homologue of a pair of chromosomes.What is the probability of this individual's child carrying the same deletion?

A) 0%
B) 25%
C) 50%
D) 75%
E) 100%

Question 5

What kinds of mutations can be revealed through ultrasound?

A) Some chromosomal abnormalities, such as Down syndrome and Edwards syndrome, and a few other known inherited disorders.
B) The genetic profile, including any mutant gene alleles the fetus may have.
C) All chromosomal mutations, including deletions, duplications, inversions, and translocations.
D) Only larger chromosomal mutations, such as the large deletion seen in individuals with cri du chat syndrome.
E) Only inherited genetic disorders caused by single gene mutations.

Question 6

A child with bluish-purple skin is found to lack the enzyme diaphorase and is subsequently diagnosed with which genetic disorder?

A) methemoglobinemia
B) Duchenne muscular dystrophy
C) Marfan syndrome
D) sickle cell disease
E) color blindness

Question 7

Figure:
You are a genetic counselor,and a man with the translocation shown in the figure is your client.He and his partner (who has a normal karyotype)wish to have children.You explain to him that the probability of having a child with an unbalanced translocation is

A) 0%.
B) 25%.
C) 50%.
D) 75%.
E) 100%.

Question 8

A genetic profile includes

A) the location of all known genes in the human genome.
B) the entire base sequence of an individual's genome.
C) all of an individual's normal genes.
D) an individual's complete genotype, including mutations.
E) all of an individual's genetic markers.

Question 9

A DNA microarray detects

A) mutant gene alleles associated with disease.
B) an individual's complete genotype, including all the various mutations.
C) chromosomal abnormalities, such as duplications or deletions.
D) fetal cells in the mother's blood.
E) viral DNA in an individual's cells.

Question 10

Amniocentesis may be preferred over chorionic villus sampling (CVS)for karyotyping because

A) CVS is a less invasive procedure and has a faster recovery time.
B) amniocentesis can be performed more quickly than CVS.
C) CVS carries a lower risk of miscarriage than amniocentesis.
D) a larger amount of tissue may be taken, allowing the results to be obtained more quickly.
E) amniocentesis may be performed at an earlier stage of pregnancy and so the risk of miscarriage is higher.

Question 11

A missing piece of chromosome 5 may result in a child whose glottis and larynx do not develop properly resulting in an abnormal cry.This is called

A) Cri du chat syndrome.
B) Huntington syndrome.
C) Klinefelter syndrome.
D) inv dup 15 syndrome.
E) Down syndrome.

Question 12

Figure:
You are a genetic counselor,and a man with the translocation shown in the figure is your client.He and his partner (who has a normal karyotype)wish to have children.You explain to him that the probability of having a child with the same translocation as the father is

A) 0%.
B) 25%.
C) 50%.
D) 75%.
E) 100%.

Question 13

A man carrying a translocation may appear normal,but runs the risk of having children with a syndrome because his children

A) may inherit both abnormal chromosomes from the father and would thus carry a deletion.
B) may inherit one abnormal chromosome with one normal one from the father, and would carry a deletion or duplication.
C) will inherit one abnormal chromosome from both the mother and father.
D) may inherit both normal chromosomes from the father and an abnormal one from the mother.
E) carry the same translocation as the father.

Question 14

Amniocentesis may be preferred over chorionic villus sampling (CVS)for karyotyping because

A) CVS takes much longer to obtain a karyotype.
B) CVS is a more invasive procedure.
C) amniocentesis has a lower risk of miscarriage than CVS.
D) amniocentesis can be performed more quickly than CVS.
E) a larger amount of tissue may be obtained through amniocentesis.

Question 15

Chromosomes for karyotyping are often obtained from a blood sample.Red blood cells,however,cannot be used for this purpose because

A) they are too small.
B) they lack nuclei.
C) white blood cells are much more common.
D) they have abnormal chromosomes.
E) they are difficult to isolate.

Question 16

Chromosome 7 may lose an end piece resulting in Williams syndrome.This is an example of a(n)

A) inversion.
B) duplication.
C) deletion.
D) translocation.
E) epigenetic inheritance.

Question 17

A known abnormality in a gene's sequence that can be linked to a genetic disease is called a(n)

A) genetic profile.
B) enzyme.
C) genetic marker.
D) DNA microarray.
E) genomic DNA.

Question 18

Figure:
You are a genetic counselor,and a man with the translocation shown in the figure is your client.He and his partner (who has a normal karyotype)wish to have children.You explain to him that the probability of having a child with a normal karyotype is

A) 0%.
B) 25%.
C) 50%.
D) 75%.
E) 100%.

Question 19

A karyotype shows chromosomes arranged by

A) banding patterns, size, and shape.
B) shape, size, and complexity.
C) complexity, radius, and length.
D) length, structure, and color.
E) color, width, and length.

Question 20

An embryo produced by in vitro fertilization (IVF)may be tested for genetic disorders prior to implantation.How is this accomplished?

A) Fetal cells are recovered from the mother's blood, and the DNA analyzed with a DNA microarray.
B) Amniocentesis or chorionic villus sampling is performed, and a karyotype assembled.
C) A polar body is isolated and its DNA amplified by PCR for analysis by DNA microarray.
D) A single cell is removed from a 6 to 8-celled embryo, and its DNA analyzed with a DNA microarray.
E) Blood is drawn from the embryo for genetic marker analysis.

Question 21

Testing for a protein may help reveal whether or not an individual has a genetic disorder.

Question 22

What are the current known methods of delivering genes to cells for gene therapy?

A) viruses, liposomes, and nasal sprays
B) viruses, nasal sprays, and gene guns
C) liposomes, nasal sprays, and chemical transformation
D) nasal sprays, liposomes, and gene guns
E) viruses and gene guns

Question 23

Mutant gene alleles associated with known genetic disorders can be detected using DNA microarray analysis.

Question 24

Transposons have not been discovered in which of the following species?

A) bacteria
B) plants
C) humans
D) fruit flies
E) fungi

Question 25

An extra three nucleotides inserted into a gene will cause a frameshift mutation.

Question 26

Which one of the following diseases or disorders has not been treated using gene therapy methods?

A) rheumatoid arthritis
B) familial hypercholesterolemia
C) cri du chat syndrome
D) sickle cell disease
E) Duchenne muscular dystrophy

Question 27

Down syndrome could not be treated by gene therapy because

A) scientists do not know which faulty genes cause the syndrome.
B) Down syndrome is caused by possessing extra copies of genes of an entire chromosome, and adding more genes would not help.
C) liposomes and nasal sprays cannot be used due to abnormalities in the respiratory tract of Down syndrome individuals.
D) there are too many genes involved in the syndrome.
E) the gene therapy treatment could not be performed on an adult individual.

Question 28

A person with familial hypercholesterolemia is participating in an ex-vivo gene therapy trial.The procedure involves

A) infecting a portion of the person's liver with a retrovirus containing a normal gene for a cholesterol receptor.
B) spraying the normal gene for the cholesterol receptor into the nose.
C) insertion of the cholesterol receptor gene into a virus, then injecting the virus into the person.
D) removing a piece of the person's liver, infecting it with a retrovirus containing the normal cholesterol receptor gene, and replacing it after treatment.
E) transplanting a normal liver into the individual.

Question 29

Which genetic disorder is due to a deletion on chromosome 7?

A) Williams syndrome
B) Cri du chat
C) Alagille syndrome
D) Down syndrome
E) cancer

Question 30

Which of the following consequences can arise as the result of a chromosomal inversion?

A) The reverse sequence of alleles can lead to altered gene activity if it disrupts the control of gene expression.
B) The additional nucleotides added to the allele can cause it to produce an additional protein.
C) The nucleotides that have been deleted from the allele will cause the new amino acid chain to be shortened.
D) The multiple copies of the adenine nucleotide that have been added will increase the number of amino acids added to the chain.
E) There are no consequences due to a chromosomal inversion.

Question 31

Mutations within genes always result in non-functional proteins.

Question 32

Ex vivo gene therapy differs from in vivo gene therapy in that

A) ex vivo gene therapy involves directly introducing the gene into the body.
B) in vivo gene therapy involves directly introducing the gene into the body.
C) in vivo gene therapy only employs viruses for gene transfer.
D) ex vivo gene therapy only employs viruses for gene transfer.
E) ex vivo gene therapy can employ viruses, nasal sprays, or liposomes for gene transfer, but only liposomes may be used for in vivo gene therapy.

Question 33

A silent mutation is more likely to occur as a result of

A) a frameshift mutation.
B) a point mutation that does not change the amino acid encoded within the gene.
C) the movement of a transposon into an exon.
D) a point mutation that alters the amino acid encoded within the gene.
E) a large dose of radiation.

Question 34

To perform an in vivo gene therapy treatment,cells are removed from the patient's body,normal genes are added to them,and then the cells are returned to the patient's body.

Question 35

During DNA replication the original strand (ATTCGCGATTTA)was replicated as (ATTCGGATTTA).What type of mutation has is present?

A) deletion
B) duplication
C) transposon
D) translocation
E) None of these mutations have taken place.

Question 36

A translocation chromosomal mutation is the exchange of segments between two homologous chromosomes.

Question 37

A transposon may cause a mutation if it

A) jumps into an exon of another gene.
B) jumps into an intron of another gene.
C) jumps into an intergenic DNA sequence.
D) remains trapped within an intergenic DNA sequence.
E) interacts with a physical mutagen.

Question 38

In what way do transposons cause mutations to occur?

A) Transposons move within and between chromosomes disrupting the genes.
B) Transposons cause large sections of the gene to be deleted from the chromosome making it useless.
C) Transposons cause sections of the chromosome to make multiple copies of the same nucleotide.
D) Transposons produce proteins that conflict with the normal functioning proteins of the cell.
E) Transposons cause nonfunctional genes to be "woken up" and become functional.

Question 39

Chorionic villus sampling carries less risk of causing miscarriage than amniocentesis.

Question 40

Mutations are uncommon because

A) DNA repair enzymes often repair errors.
B) physical mutagens such as X-rays seldom damage DNA.
C) DNA is able to repair itself over time.
D) frameshift mutations occur very frequently.
E) transposons are constantly moving throughout the genome.

Question 41

What structure is often used to deliver copies of genes into cells?

A) viruses
B) PCR
C) bacteria
D) prions
E) hypodermic needles

Question 42

Which human disorder is not being treated with gene therapy?

A) severe combined immunodeficiency (SCID)
B) familial hypercholesterolemia
C) cancer
D) cystic fibrosis
E) All of these are being treated with gene therapy.

Question 43

Which type of chromosomal mutation will lead to Alagille syndrome?

A) translocation
B) duplication
C) inversion
D) frameshift
E) point mutation

Question 44

In hemoglobin,the shift from glutamic acid to valine is considered what type of mutation?

A) point mutation
B) frameshift mutation
C) transposons
D) deletion
E) duplication

Question 45

Which structure is used in the new treatment of rheumatoid arthritis?

A) adenovirus
B) SCID
C) bacteriophage
D) hypodermic needles
E) None of these structures are used in the treatment of rheumatoid arthritis.