Deck 22: Genetics and Genetically Linked Diseases
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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.
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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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
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
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
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
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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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.
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17
_________________________ is a disease characterized by chronic bronchitis and pneumonia.
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18
Intentionally introducing new characteristics or attributes into an organism is known as genetic engineering.
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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
A) identifying techniques to correct faulty genes
B) lack of information about human genetic material
C) the body's natural immune response
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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.
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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
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
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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
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
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23
The probable reason why certain genetic diseases are more common among specific ethnic groups is that the group members share a similar _________________________.
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24
The technique for correcting defective genes that cause disease is called ______________________________.
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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
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
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26
It is estimated that everyone carries two or three recessive ____________________ genes.
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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
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
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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
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
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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
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
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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
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
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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
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
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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
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
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33
The ____________________ is a small functional unit of DNA that carries instructions for cellular synthesis of a specific protein.
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34
The modification of genes outside an organism's natural reproductive process is called ______________________________.
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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
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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