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Topic 2: Genes and Health
2.6 Genetic Screening and Counseling
2.6.2 Carrier Testing
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What is the purpose of carrier testing?
Identifies mutated allele carriers
Carriers of a mutated allele exhibit symptoms of the disease.
False
A carrier of the gene for cystic fibrosis has one normal allele
C
F
CF
CF
and one mutated allele cf
Why is carrier testing valuable for couples planning to have children?
Informed family planning
Carriers of a mutated allele have one normal and one mutated
allele
What is the genotype of a carrier for cystic fibrosis?
C
f
Cf
C
f
Steps in the process of carrier testing
1️⃣ Sample collection
2️⃣ DNA extraction
3️⃣ Amplification (if needed)
4️⃣ Detection of mutated allele
5️⃣ Result interpretation
Individuals with a family history of a genetic disorder should consider carrier
testing
Couples planning to have children should consider carrier testing, especially if there's a known
genetic
condition in either family.
What is the reason for carrier testing in individuals with a family history of a genetic disorder?
Understand the risk
What is the reason for carrier testing in couples planning to have children?
Assess inheritance risk
Why might a couple with a family history of cystic fibrosis consider carrier testing?
Understand their risk
Match the type of carrier testing with its focus:
Single-gene testing ↔️ Specific genetic disorder
Expanded panel testing ↔️ Multiple disorders simultaneously
Ethnicity-based testing ↔️ Disorders common in ethnic groups
Ethnicity-based testing is used to detect disorders more common in specific ethnic
populations
A couple of Ashkenazi Jewish descent might opt for ethnicity-based carrier testing to assess their risk of passing on
Tay-Sachs
disease.
What is the primary purpose of carrier testing in family planning?
Understand inheritance likelihood
What is a carrier in carrier testing?
One normal, one mutated allele
A cystic fibrosis carrier has the genotype
C
f
Cf
C
f
.
The main purpose of carrier testing is to identify individuals who carry a mutated
allele
What is the primary purpose of risk assessment in carrier testing?
Understanding inheritance likelihood
Match the purpose of carrier testing with its explanation.
1️⃣ Risk Assessment
2️⃣ Determines the probability of offspring inheriting a genetic condition
3️⃣ Family Planning
4️⃣ Guides decisions about conceiving, adopting, or using reproductive technologies
If both parents are carriers for cystic fibrosis, their child has a
25%
chance of developing the disease.
Who should consider carrier testing?
Those with a family history
Match the group with the reason for carrier testing.
Family history of genetic disorder ↔️ Understand risk of passing condition
Couples planning to have children ↔️ Assess risk of child inheriting condition
Single-gene testing focuses on detecting carriers for a specific genetic
disorder
Which type of carrier testing targets disorders common in specific ethnic populations?
Ethnicity-based testing
Steps in the process of carrier testing.
1️⃣ Sample Collection
2️⃣ DNA Isolation
3️⃣ Genetic Analysis
4️⃣ Result Interpretation
For which gene are mutations analyzed in cystic fibrosis carrier testing?
CFTR
Ethical considerations in carrier testing include informed consent, privacy, and
psychological
impact.
What does informed consent ensure in carrier testing?
Understanding testing implications
Psychological impact in carrier testing refers to managing the emotional effects of test
results
Match the ethical consideration with its description.
Informed Consent ↔️ Understanding testing implications
Privacy ↔️ Protecting genetic information
Psychological Impact ↔️ Managing emotional effects of results
What does a positive result in carrier testing indicate?
Carries mutated allele
If both parents test positive for a recessive genetic disorder, their child has a
50%
chance of being a carrier.
What genotype does a carrier of cystic fibrosis have?
C
f
Cf
C
f
Family planning in carrier testing allows couples to make informed decisions about having
children
Why should couples planning to have children consider carrier testing?
Assess risk of child inheriting
If both parents are carriers for cystic fibrosis, there is a
25%
chance their child will develop the disease.
Understanding their carrier status helps individuals make informed decisions about
family
planning.
Match the group with their reason for carrier testing:
Family history of genetic disorder ↔️ To understand the risk of passing on the condition
Couples planning to have children ↔️ To assess the risk of their child inheriting a genetic condition
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