a. Define the following terms: gene,
DNA, chromosome, autosome, sex
chromosome.
b. Summarize the chromosomal makeup
of a human cell to include 1) the number of
chromosomes, 2) the number of
autosomes and sex chromosomes, 3) the
differentiation of gender by
chromosomes.
c. Describe how gene mutations are
linked to disease.
d. Differentiate between a
hereditary mutation and an acquired mutation.
g. Define recessive allele, dominant
allele, and carrier.
h. Discuss how a recessive or
dominant allele affects the hereditary influence of
a disease.
i. Illustrate the following
inheritance patterns using a punnett square:
autosomal dominant, autosomal recessive, sex-linked
recessive.
j. Discuss the percentage and sex of
the offspring affected in autosomal dominant,
autosomal recessive, and sex-linked recessive
disease.
k. Define gene testing and
predictive gene testing. List benefits, risks,
and limitations of genetic testing.
3. Define which hemostasis function(s)
is/are tested for in each of the following tests.
4 Define hemophilia.
5. List the symptoms of a patient with
hemophilia to include complications that may arise
from symptoms.
6. Summarize treatments of a hemophilia
to include:
a. the goals of treatment.
b. Discuss the process by which
recombinant factor VIII is made.
c. Discuss blood borne diseases and
their impact on an individual with hemophilia.
d. Describe how gene therapy may
become a cure for hemophilia.
7. Discuss the roles of a pediatrician
and/or hematologist, nurses, clinical laboratory
scientists, and genetic counselors in diagnosing and
treating a patient with hemophilia.
8. Define how an individual with hemophilia can stop
the transmission of the disease.