# Situation: A nurse assists in the genetic counseling and fertility clinic of a medical center, where couples come for preconception advice. A couple are both carriers of beta-thalassemia, an autosomal recessive disorder. Their first child has beta-thalassemia major. Their second child has been shown not to have the disease, but carrier testing has not been done. What is the probability that the second child is a carrier? Round off to the nearest whole percent.

> source: MyMerci (mymerci.kr)  
> url: https://mymerci.kr/pages/nclex_q.php?qn_id=629499  
> language: ko  
> subject: Nursing Practice II — Maternal and Child Health Nursing

## 문제

Situation: A nurse assists in the genetic counseling and fertility clinic of a medical center, where couples come for preconception advice.

A couple are both carriers of beta-thalassemia, an autosomal recessive disorder. Their first child has beta-thalassemia major. Their second child has been shown not to have the disease, but carrier testing has not been done. What is the probability that the second child is a carrier? Round off to the nearest whole percent.

## 보기

1. 25%
2. 50%
3. 67% **✔ 정답**
4. 75%

**정답: 3**

## 해설

When both parents are carriers of an autosomal recessive disorder, each pregnancy has a 25% chance of an affected child, 50% of a carrier, and 25% of a noncarrier. Because this child is known to be unaffected, only the three unaffected outcomes remain, and two of those three are carriers. The probability is 2/3, or about 67%.

## 심화 해설

Conditional probability in autosomal recessive inheritance

Both parents are carriers of beta-thalassemia, meaning each has one normal beta-globin allele and one mutated allele. For any pregnancy, the possible combinations from two carrier parents follow a predictable pattern: 25% chance the child inherits two mutated alleles and has beta-thalassemia major, 50% chance the child inherits one mutated allele and is a carrier, and 25% chance the child inherits two normal alleles and is neither affected nor a carrier.

The key detail in this scenario is that the second child has already been shown not to have the disease. This removes the 25% affected outcome from consideration. The remaining possibilities are the three unaffected genotypes: two of these are carriers, and one is a noncarrier. Because the child is known to be unaffected, the probability of being a carrier is calculated only among the unaffected outcomes, giving 2 out of 3, or approximately 67%.

| Genotype | Alleles inherited | Clinical status | Included after knowing child is unaffected? |
| --- | --- | --- | --- |
| Homozygous normal | Normal + Normal | Unaffected, noncarrier | Yes (1 of 3 remaining) |
| Heterozygous carrier | Normal + Mutated | Unaffected, carrier | Yes (2 of 3 remaining) |
| Homozygous mutated | Mutated + Mutated | Beta-thalassemia major | No (excluded) |

Watch out! A common error is to answer 50% by recalling the general carrier probability for any pregnancy before knowing the child's phenotype. However, once the child is confirmed unaffected, the affected 25% is eliminated, and the denominator changes from 4 to 3. The probability of being a carrier among unaffected children is 2/3, not 1/2.

This principle applies to any autosomal recessive condition when a child is known to be unaffected but carrier status is unknown. In thalassemia, carrier detection is clinically relevant because carriers may have mild microcytic anemia that can be mistaken for iron deficiency. According to the rapid evidence review, thalassemia should be suspected in patients with microcytic anemia and normal or elevated ferritin levels, which distinguishes it from iron deficiency anemia where ferritin is typically low [1]. Carrier screening programs for thalassemia and other hemoglobinopathies are offered to people considering pregnancy or who are pregnant, allowing couples to understand reproductive risks before conception .

Key point! For autosomal recessive disorders, when a child is known to be unaffected, the carrier probability among unaffected siblings is always 2/3 (about 67%), regardless of which specific recessive condition is involved.References (research sources)

- [1]Alpha- and Beta-thalassemia: Rapid Evidence Review.Research articleBaird DC, Batten SH, Sparks SK (2022)

## 임상 시나리오

Conditional Carrier Risk in Autosomal Recessive InheritanceRecalculating probability after phenotype is known
When both parents are carriers of an autosomal recessive disorder, each pregnancy has a 25% chance of an affected child, 50% chance of a carrier, and 25% chance of a noncarrier. If a child is confirmed unaffected, the affected 25% is excluded, leaving three equally likely outcomes: two carrier genotypes and one noncarrier genotype.

The probability that an unaffected child is a carrier is therefore 2/3, or approximately 67%. This is a conditional probability because it is calculated only among the remaining unaffected outcomes, not among all possible pregnancies.

CautionDo not answer 50% by recalling the general carrier probability before phenotype is known. Once the child is known to be unaffected, the affected genotype is eliminated from the denominator, shifting the carrier probability to 67%.

## 핵심 개념

- **Autosomal recessive** — Inheritance pattern requiring two mutated alleles for disease expression; carriers have one normal and one mutated allele.
- **Carrier** — An individual with one normal and one mutated allele for a recessive condition, typically unaffected.
- **Conditional probability** — Probability of an event given that another event has occurred; here, carrier status given the child is unaffected.
- **Beta-thalassemia major** — Severe form of beta-thalassemia resulting from inheriting two mutated beta-globin alleles.
- **Genotype** — The genetic makeup of an individual; for carrier parents, offspring genotypes follow a 1:2:1 ratio.

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