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Answer: B
Recombinant DNA is the practice of altering/manipulating, recombining and reorganizing living tissue into new forms and
shapes.
Answer: A
Gene testing is generally performed for the following reasons:
- Conformational diagnosis for a symptomatic individual
- Presymptomatic testing for estimating risk of developing disease
- Presymptomatic testing for predicting disease
- Prenatal diagnosis screening
- Newborn screening
- Preimplantation genetic diagnosis
- Carrier screening
- Forensic screening
- Paternal testing
3. In 2008, this act was passed to protect individuals from genetic discrimination by health insurers and employers.
A. HIPAA
B. EMTALA
C. GINA
D. BAIPA
Answer: C
In 2008, Genetic Information Nondiscrimination Act (GINA) passed protecting individuals from genetic discrimination by
health insurers and employers. GINA Prohibits the following:
- Health Insurers may not use a person’s genetic information in determining eligibility or premiums.
- Health insurers may not request or require that a person undergo a genetic test for underwriting decisions.
- Employers may not use a person’s genetic information in making employment decisions such as hiring, firing, job
assignment, or any other terms of employment.
- Employers may not request, require, or purchase genetic information about a person or their family members.
Answer: D
Genetic predisposition is a genetically determined susceptibility to certain health problems. It does not cause the disease
itself but, in combination and behavioral environmental factors, can increase a person’s chances of getting a certain
disease.
5. This is a disease that deforms red blood cells into thin, elongated sickle-shaped forms and causes anemia, cough,
and muscle cramps.
A. Sickle cell disease
B. Pernicious anemia
C. Down syndrome
D. Huntington disease
Answer: A
Sickle cell disease is a genetic disease that deforms red blood cells into thin, elongated sickle-shaped forms and causes
anemia, cough, and muscle cramps. Sickle cell occurs only when both parents are genetic carrier of the recessive gene. If
both parents are carriers, there is a 25 percent chance that the child will have the disease.