If both parents are carriers of thalassemia, which is an autosomal recessive disorder, what are the chances of pregnancy resulting in an affected child?
Correct answer: A. 25%
- A. 25%
- B. 100%
- C. No chance
- D. 50%
Explanation
Thalassemia is an autosomal recessive disorder, meaning an affected child must inherit two recessive alleles (tt), one from each parent. If both parents are carriers (Tt), they have a 25% chance of producing a child with two recessive alleles (tt) and thus affected by thalassemia. The Punnett square for Tt x Tt yields the genotypic ratio: 1 TT : 2 Tt : 1 tt, where only the tt genotype results in an affected child. Therefore, the chance of an affected child is 25%. Option A is correct. Other options provide incorrect probabilities for carriers or unaffected children.
Report an error
The more specific you are, the faster it gets fixed. A source beats an opinion.
Prefer email? [email protected]
About Inheritance
Mendel's laws explain segregation, independent assortment and the prediction of genetic ratios using alleles, genotypes and phenotypes. The chapter also covers linked genes, recombination and crossing over during meiosis, then applies pedigree reasoning to X-linked recessive traits, which show different inheritance patterns in males and females.
Practise Inheritance
1,238 free Inheritance MCQs from Biology, each with the correct answer and an explanation. Unlimited attempts, no account needed.
Discussion
Stuck on an option, or know a faster way to get there? Ask or explain it here.
No comments yet. Be the first to explain this one.
Exams that ask Biology questions like this
Biology is on 8 papers prepared for on TestUstad, and all of them draw the same bank, so this question is worth knowing for every one of them.
More Inheritance questions
A man with blood group A marries a woman with blood group B. What are all the possible blood groups of their offspring?
The movement of a gene from one linkage group to another is called:
A pleiotropic gene:
Down's syndrome in humans is due to:
F2 generation in a Mendelian cross showed that both genotypic and phenotypic ratios are the same as 1 : 2 : 1 and offspring are intermediate of both parents. It represents a case of:
A test cross is carried out to: