Deck 22: Genetics and Genetically Linked Diseases

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Question
Down syndrome is sometimes referred to as trisomy 21.​
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Question
Which of the following is a causative factor in the abnormal development of sexual organs?​

A) ​An extra chromosome exists.
B) ​Sex chromosomes do not split apart when gametes are formed.
C) ​The genes for sexual development are missing.
Question
Most inherited mutated genes pass on a beneficial characteristic.​
Question
____________________ is the branch of biology that studies how the genes are transmitted from parents to offspring.​
Question
A(n)____________________ disorder is caused by a variation in the genetic pattern.​
Question
What is chorionic villi sampling?​

A) ​Diagnostic test in which fetal cells are removed from the placenta and examined
B) ​Test performed on amniotic fluid to identify potential disorders
C) ​Questionnaire used in genetic counseling to create a family history
D) ​Test given to newborn infants to identify the presence of phenylketonuria
Question
Radiation and the chemical benzene are examples of _________________________ agents.​
Question
A mutagenic agent _____.​

A) ​helps prevent mutations
B) ​causes mutations in many cells at the same time
C) ​slows down the rate of mutation
D) ​increases the occurrence of mutations
Question
When parents share similar gene pools,their chances of having spontaneous abortions and stillbirths increase.​
Question
Skin cells that undergo random changes as a person ages provide an example of a(n)_____ mutation.​

A) ​chromosomal
B) ​gene
C) ​somatic
D) ​inherited
Question
____________________ is the term for a change that occurs in the nucleus of gametes,and is passed on to the next generation.​
Question
____________________ is a sex-linked blood disorder passed on the X chromosome.​
Question
A genetic disorder is the same as a congenital disorder.​
Question
What is the purpose of a determining a person's genotype?​

A) ​Finding possible cures for genetic disorders
B) ​Mapping all the genes of the human body
C) ​Predicting the possibility of a genetic disorder
D) ​Locating common sites of genetic mutations
Question
Genetic counseling is recommended for women who are pregnant after age 40.​
Question
______________________________ helps prospective parents make informed decisions about having children.​
Question
_________________________ is a disease characterized by chronic bronchitis and pneumonia.​
Question
Intentionally introducing new characteristics or attributes into an organism is known as genetic engineering.​
Question
A major factor that must be overcome for gene therapy to become an effective treatment option is _____.​

A) ​identifying techniques to correct faulty genes
B) ​lack of information about human genetic material
C) ​the body's natural immune response
Question
Lethal genes can cause death at any time during the human life cycle,from the zygote stage to a mature adult human being.​
Question
Match each disorder with its description.​
a.​phenylketonuria
b.​sickle cell anemia
c.​Tay-Sachs disease
d.​Duchenne's muscular dystrophy
e.​Huntington's disease
f.​cystic fibrosis
g.​thalassemia
h.​hemophilia
i.​Down syndrome
j.Turner's syndrome
​inability to produce a substance necessary for blood clotting
Question
Match each disorder with its description.​
a.​phenylketonuria
b.​sickle cell anemia
c.​Tay-Sachs disease
d.​Duchenne's muscular dystrophy
e.​Huntington's disease
f.​cystic fibrosis
g.​thalassemia
h.​hemophilia
i.​Down syndrome
j.Turner's syndrome
​abnormal gene causes deterioration of the central nervous system
Question
The probable reason why certain genetic diseases are more common among specific ethnic groups is that the group members share a similar _________________________.​
Question
​The technique for correcting defective genes that cause disease is called ______________________________.
Question
Match each disorder with its description.​
a.​phenylketonuria
b.​sickle cell anemia
c.​Tay-Sachs disease
d.​Duchenne's muscular dystrophy
e.​Huntington's disease
f.​cystic fibrosis
g.​thalassemia
h.​hemophilia
i.​Down syndrome
j.Turner's syndrome
​excretion of thick mucus that blocks the respiratory passages
Question
It is estimated that everyone carries two or three recessive ____________________ genes.​
Question
Match each disorder with its description.​
a.​phenylketonuria
b.​sickle cell anemia
c.​Tay-Sachs disease
d.​Duchenne's muscular dystrophy
e.​Huntington's disease
f.​cystic fibrosis
g.​thalassemia
h.​hemophilia
i.​Down syndrome
j.Turner's syndrome
​missing enzyme causes brain damage that results in mental and motor deterioration
Question
Match each disorder with its description.​
a.​phenylketonuria
b.​sickle cell anemia
c.​Tay-Sachs disease
d.​Duchenne's muscular dystrophy
e.​Huntington's disease
f.​cystic fibrosis
g.​thalassemia
h.​hemophilia
i.​Down syndrome
j.Turner's syndrome
​anemia accompanied by enlargement of the spleen and possible congestive heart disease
Question
Match each disorder with its description.​
a.​phenylketonuria
b.​sickle cell anemia
c.​Tay-Sachs disease
d.​Duchenne's muscular dystrophy
e.​Huntington's disease
f.​cystic fibrosis
g.​thalassemia
h.​hemophilia
i.​Down syndrome
j.Turner's syndrome
​presence of an extra chromosome,which causes certain physical malformations and some degree of mental retardation
Question
Match each disorder with its description.​
a.​phenylketonuria
b.​sickle cell anemia
c.​Tay-Sachs disease
d.​Duchenne's muscular dystrophy
e.​Huntington's disease
f.​cystic fibrosis
g.​thalassemia
h.​hemophilia
i.​Down syndrome
j.Turner's syndrome
​a chromosomal nondisjunction that results in abnormal female sexual development
Question
Match each disorder with its description.​
a.​phenylketonuria
b.​sickle cell anemia
c.​Tay-Sachs disease
d.​Duchenne's muscular dystrophy
e.​Huntington's disease
f.​cystic fibrosis
g.​thalassemia
h.​hemophilia
i.​Down syndrome
j.Turner's syndrome
​metabolic disorder that disrupts normal brain development
Question
Match each disorder with its description.​
a.​phenylketonuria
b.​sickle cell anemia
c.​Tay-Sachs disease
d.​Duchenne's muscular dystrophy
e.​Huntington's disease
f.​cystic fibrosis
g.​thalassemia
h.​hemophilia
i.​Down syndrome
j.Turner's syndrome
​abnormality of red blood cells interfering with ability to carry oxygen
Question
The ____________________ is a small functional unit of DNA that carries instructions for cellular synthesis of a specific protein.​
Question
The modification of genes outside an organism's natural reproductive process is called ______________________________.​
Question
Match each disorder with its description.​
a.​phenylketonuria
b.​sickle cell anemia
c.​Tay-Sachs disease
d.​Duchenne's muscular dystrophy
e.​Huntington's disease
f.​cystic fibrosis
g.​thalassemia
h.​hemophilia
i.​Down syndrome
j.Turner's syndrome
​impairment of skeletal muscles in which their fibers are replaced with fat and connective tissue
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Deck 22: Genetics and Genetically Linked Diseases
1
Down syndrome is sometimes referred to as trisomy 21.​
True
2
Which of the following is a causative factor in the abnormal development of sexual organs?​

A) ​An extra chromosome exists.
B) ​Sex chromosomes do not split apart when gametes are formed.
C) ​The genes for sexual development are missing.
B
3
Most inherited mutated genes pass on a beneficial characteristic.​
False
4
____________________ is the branch of biology that studies how the genes are transmitted from parents to offspring.​
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5
A(n)____________________ disorder is caused by a variation in the genetic pattern.​
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Unlock for access to all 35 flashcards in this deck.
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6
What is chorionic villi sampling?​

A) ​Diagnostic test in which fetal cells are removed from the placenta and examined
B) ​Test performed on amniotic fluid to identify potential disorders
C) ​Questionnaire used in genetic counseling to create a family history
D) ​Test given to newborn infants to identify the presence of phenylketonuria
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7
Radiation and the chemical benzene are examples of _________________________ agents.​
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8
A mutagenic agent _____.​

A) ​helps prevent mutations
B) ​causes mutations in many cells at the same time
C) ​slows down the rate of mutation
D) ​increases the occurrence of mutations
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9
When parents share similar gene pools,their chances of having spontaneous abortions and stillbirths increase.​
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10
Skin cells that undergo random changes as a person ages provide an example of a(n)_____ mutation.​

A) ​chromosomal
B) ​gene
C) ​somatic
D) ​inherited
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11
____________________ is the term for a change that occurs in the nucleus of gametes,and is passed on to the next generation.​
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12
____________________ is a sex-linked blood disorder passed on the X chromosome.​
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13
A genetic disorder is the same as a congenital disorder.​
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14
What is the purpose of a determining a person's genotype?​

A) ​Finding possible cures for genetic disorders
B) ​Mapping all the genes of the human body
C) ​Predicting the possibility of a genetic disorder
D) ​Locating common sites of genetic mutations
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Unlock for access to all 35 flashcards in this deck.
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15
Genetic counseling is recommended for women who are pregnant after age 40.​
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16
______________________________ helps prospective parents make informed decisions about having children.​
Unlock Deck
Unlock for access to all 35 flashcards in this deck.
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k this deck
17
_________________________ is a disease characterized by chronic bronchitis and pneumonia.​
Unlock Deck
Unlock for access to all 35 flashcards in this deck.
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18
Intentionally introducing new characteristics or attributes into an organism is known as genetic engineering.​
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Unlock for access to all 35 flashcards in this deck.
Unlock Deck
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19
A major factor that must be overcome for gene therapy to become an effective treatment option is _____.​

A) ​identifying techniques to correct faulty genes
B) ​lack of information about human genetic material
C) ​the body's natural immune response
Unlock Deck
Unlock for access to all 35 flashcards in this deck.
Unlock Deck
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20
Lethal genes can cause death at any time during the human life cycle,from the zygote stage to a mature adult human being.​
Unlock Deck
Unlock for access to all 35 flashcards in this deck.
Unlock Deck
k this deck
21
Match each disorder with its description.​
a.​phenylketonuria
b.​sickle cell anemia
c.​Tay-Sachs disease
d.​Duchenne's muscular dystrophy
e.​Huntington's disease
f.​cystic fibrosis
g.​thalassemia
h.​hemophilia
i.​Down syndrome
j.Turner's syndrome
​inability to produce a substance necessary for blood clotting
Unlock Deck
Unlock for access to all 35 flashcards in this deck.
Unlock Deck
k this deck
22
Match each disorder with its description.​
a.​phenylketonuria
b.​sickle cell anemia
c.​Tay-Sachs disease
d.​Duchenne's muscular dystrophy
e.​Huntington's disease
f.​cystic fibrosis
g.​thalassemia
h.​hemophilia
i.​Down syndrome
j.Turner's syndrome
​abnormal gene causes deterioration of the central nervous system
Unlock Deck
Unlock for access to all 35 flashcards in this deck.
Unlock Deck
k this deck
23
The probable reason why certain genetic diseases are more common among specific ethnic groups is that the group members share a similar _________________________.​
Unlock Deck
Unlock for access to all 35 flashcards in this deck.
Unlock Deck
k this deck
24
​The technique for correcting defective genes that cause disease is called ______________________________.
Unlock Deck
Unlock for access to all 35 flashcards in this deck.
Unlock Deck
k this deck
25
Match each disorder with its description.​
a.​phenylketonuria
b.​sickle cell anemia
c.​Tay-Sachs disease
d.​Duchenne's muscular dystrophy
e.​Huntington's disease
f.​cystic fibrosis
g.​thalassemia
h.​hemophilia
i.​Down syndrome
j.Turner's syndrome
​excretion of thick mucus that blocks the respiratory passages
Unlock Deck
Unlock for access to all 35 flashcards in this deck.
Unlock Deck
k this deck
26
It is estimated that everyone carries two or three recessive ____________________ genes.​
Unlock Deck
Unlock for access to all 35 flashcards in this deck.
Unlock Deck
k this deck
27
Match each disorder with its description.​
a.​phenylketonuria
b.​sickle cell anemia
c.​Tay-Sachs disease
d.​Duchenne's muscular dystrophy
e.​Huntington's disease
f.​cystic fibrosis
g.​thalassemia
h.​hemophilia
i.​Down syndrome
j.Turner's syndrome
​missing enzyme causes brain damage that results in mental and motor deterioration
Unlock Deck
Unlock for access to all 35 flashcards in this deck.
Unlock Deck
k this deck
28
Match each disorder with its description.​
a.​phenylketonuria
b.​sickle cell anemia
c.​Tay-Sachs disease
d.​Duchenne's muscular dystrophy
e.​Huntington's disease
f.​cystic fibrosis
g.​thalassemia
h.​hemophilia
i.​Down syndrome
j.Turner's syndrome
​anemia accompanied by enlargement of the spleen and possible congestive heart disease
Unlock Deck
Unlock for access to all 35 flashcards in this deck.
Unlock Deck
k this deck
29
Match each disorder with its description.​
a.​phenylketonuria
b.​sickle cell anemia
c.​Tay-Sachs disease
d.​Duchenne's muscular dystrophy
e.​Huntington's disease
f.​cystic fibrosis
g.​thalassemia
h.​hemophilia
i.​Down syndrome
j.Turner's syndrome
​presence of an extra chromosome,which causes certain physical malformations and some degree of mental retardation
Unlock Deck
Unlock for access to all 35 flashcards in this deck.
Unlock Deck
k this deck
30
Match each disorder with its description.​
a.​phenylketonuria
b.​sickle cell anemia
c.​Tay-Sachs disease
d.​Duchenne's muscular dystrophy
e.​Huntington's disease
f.​cystic fibrosis
g.​thalassemia
h.​hemophilia
i.​Down syndrome
j.Turner's syndrome
​a chromosomal nondisjunction that results in abnormal female sexual development
Unlock Deck
Unlock for access to all 35 flashcards in this deck.
Unlock Deck
k this deck
31
Match each disorder with its description.​
a.​phenylketonuria
b.​sickle cell anemia
c.​Tay-Sachs disease
d.​Duchenne's muscular dystrophy
e.​Huntington's disease
f.​cystic fibrosis
g.​thalassemia
h.​hemophilia
i.​Down syndrome
j.Turner's syndrome
​metabolic disorder that disrupts normal brain development
Unlock Deck
Unlock for access to all 35 flashcards in this deck.
Unlock Deck
k this deck
32
Match each disorder with its description.​
a.​phenylketonuria
b.​sickle cell anemia
c.​Tay-Sachs disease
d.​Duchenne's muscular dystrophy
e.​Huntington's disease
f.​cystic fibrosis
g.​thalassemia
h.​hemophilia
i.​Down syndrome
j.Turner's syndrome
​abnormality of red blood cells interfering with ability to carry oxygen
Unlock Deck
Unlock for access to all 35 flashcards in this deck.
Unlock Deck
k this deck
33
The ____________________ is a small functional unit of DNA that carries instructions for cellular synthesis of a specific protein.​
Unlock Deck
Unlock for access to all 35 flashcards in this deck.
Unlock Deck
k this deck
34
The modification of genes outside an organism's natural reproductive process is called ______________________________.​
Unlock Deck
Unlock for access to all 35 flashcards in this deck.
Unlock Deck
k this deck
35
Match each disorder with its description.​
a.​phenylketonuria
b.​sickle cell anemia
c.​Tay-Sachs disease
d.​Duchenne's muscular dystrophy
e.​Huntington's disease
f.​cystic fibrosis
g.​thalassemia
h.​hemophilia
i.​Down syndrome
j.Turner's syndrome
​impairment of skeletal muscles in which their fibers are replaced with fat and connective tissue
Unlock Deck
Unlock for access to all 35 flashcards in this deck.
Unlock Deck
k this deck
locked card icon
Unlock Deck
Unlock for access to all 35 flashcards in this deck.