To solve the question of determining the probability of having an affected child when both parents are carriers of thalassaemia, we need to understand the genetics behind autosomal recessive disorders.
Step 1: Understand the Genetics Involved
Thalassaemia is an autosomal recessive genetic disorder. This means that a person needs to receive two copies of the mutant gene (one from each parent) to exhibit symptoms of the disorder. Here are the genetic possibilities for the offspring when both parents are carriers.
Step 2: Set up a Punnett Square
Using a Punnett square, we can calculate the probability of the possible genotypes of the children.
| \(A\) | \(a\) | |
|---|---|---|
| \(A\) | \(AA\) | \(Aa\) |
| \(a\) | \(Aa\) | \(aa\) |
Step 3: Analyze the Chances
The Punnett square reveals:
Conclusion: The chance of the pregnancy resulting in a child affected by thalassaemia is \(25\%\). Thus, the correct answer is \(25\%\).