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WGU D115 Unit 2 Questions and Answers 2023 (Verified Answers)

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WGU D115 Unit 2 Questions and Answers 2023 (Verified Answers) Which type of genetic disease affects males more frequently than females? Sex-linked recessive Autosomal recessive Autosomal dominant Sex-linked dominant Sex-Linked recessive. Since males only have one X and one Y, if the affec...

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  • March 3, 2023
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WGU D115 Unit 2 Questions and Answers 2023 (Verified
Answers)
Which type of genetic disease affects males more frequently than females?

Sex-linked recessive
Autosomal recessive
Autosomal dominant
Sex-linked dominant
Sex-Linked recessive. Since males only have one X and one Y, if the affected
chromosome has the illness, it will be expressed.
In which two conditions are chromosomal abnormalities the leading known
cause?

Intellectual disability
Respiratory disorders
Fetal miscarriage
Cardiovascular disease
Mental illness
Check My Answer
Intellectual disability and fetal miscarriage. Chromosome abnormalities are the leading
known cause of intellectual disability and fetal miscarriage.
What are three examples of prenatal diagnostic studies?
Drug-sensitivity testing
Chorionic villus sampling (CVS)
Microscopy of cervical mucosa
Preimplantation genetic testing (PGT)
Amniocentesis
Chorionic villus sampling (CVS), amniocentesis, and preimplantation genetic testing
(PGT) are examples of prenatal diagnostic studies and are performed in vitro. CVS is a
form of genetic testing that provides genetic information found in utero and is usually
performed between weeks 11 and 14 of pregnancy. An amniocentesis is a form of
genetic testing that evaluates amniotic fluid and is usually performed during the second
trimester, between weeks 15 and 20 of pregnancy. PGT is performed on the embryo
prior to implantation.
Which genetic disorder is characterized by the presence of a zygote having one
chromosome with a normal complement of genes and one chromosome with a
missing gene?
Klinefelter syndrome
Down syndrome
Cri du chat syndrome
Turner syndrome
Cri du chat syndrome (translated as "cry of the cat") is caused by a DNA deletion. This
term describes the cry often heard from a baby affected by the syndrome. Cri du chat
syndrome can present as a microcephalic, low birth-weight baby with a piercing cry.

, How can an X-linked recessive disease skip generations?

Mothers cannot pass X-linked genes to their sons.
Females are hemizygous for the X chromosome.
The disease can be transmitted through female carriers.
These diseases need only one copy of the gene in females.
The disease can be transmitted through female carriers.

Since females have two copies of the X chromosome, the mother may provide an
unaffected X to a daughter or son. Furthermore, a daughter may not show signs of the
disease because she has the other X (the only X the father can give to a female) to
cancel it out.
Which type of risk is referred to as the ratio of the disease rate among the entire
population to the disease rate in an unexposed population?
Relative
Attributable
Contingency
Causal
Relative risk is a ratio of probability, not an actual occurrence of disease.
What are the empirical risks for most multifactorial diseases based on?

Direct observation
Chromosomal testing
Relative risks
Liability thresholds
Many factors from lifestyle to genetics affect multifactorial diseases. Observation and
evaluation of each case individually provides the most thorough and accurate
assessment.
What refers to the silenced gene of a gene pair.

Imprinted, activated, mutated, altered
The imprinted gene is the silent gene of a gene pair.
What is the primary reason that some older adults have impaired inflammation
and wound healing?
The circulatory system cannot adequately perfuse tissues.
The underlying chronic illness exists.
The complement is deficient.
The number of mast cells is insufficient.
The underlying chronic illness exists.
A generalized inflammatory response seen in chronic illness depletes the body's
reserves to fight against illness.
Which cells are the body's primary defense against parasite invasion?
B lymphocytes
Eosinophils
Neutrophils
T lymphocytes

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