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Thalassemia is an inherited anemic disorder in humans. Affected individuals exhibit either a minor anemia or a major anemia. Assuming that only a single gene pair and two alleles are involved in the inheritance of these conditions, is thalassemia a dominant or recessive disorder?

Short Answer

Expert verified
Answer: Thalassemia is a recessive disorder.

Step by step solution

01

Understand the context of dominant and recessive traits

Dominant traits are those that are expressed when an organism has at least one dominant allele in its genotype. In other words, whether an individual carries one or two copies of the dominant allele, the trait will be present. On the other hand, a recessive trait is only expressed when an organism has two copies of the recessive allele in its genotype. If an individual carries only one copy of the recessive allele and one copy of the dominant allele, the dominant trait is expressed.
02

Analyze the inheritance patterns in thalassemia

Thalassemia presents itself in two forms: minor anemia and major anemia. We can assume that major anemia is the more severe, expressed form of the disorder, and minor anemia is the less severe, partially affected state.
03

Compare the inheritance patterns to dominant and recessive traits

Since there are individuals exhibiting two different expressions of anemia (major and minor), it is likely that these represent heterozygous and homozygous genotypes for the responsible allele. If thalassemia were a dominant disorder, we would expect both affected individuals carrying one copy (heterozygous) and those carrying two copies (homozygous) of the dominant allele to exhibit major anemia. However, this is not observed. Instead, individuals with minor anemia likely carry only one copy of the responsible allele, while those with major anemia inherit two copies. This pattern of inheritance is consistent with a recessive trait, where only those with two copies of the recessive allele exhibit the fully affected state.
04

Conclusion

Based on the inheritance patterns observed in thalassemia, it is more likely that thalassemia is a recessive disorder, as individuals with one copy of the responsible allele express minor anemia, while those with two copies exhibit major anemia.

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Most popular questions from this chapter

Two true-breeding pea plants were crossed. One parent is round, terminal, violet, constricted, while the other expresses the respective contrasting phenotypes of wrinkled, axial, white, full. The four pairs of contrasting traits are controlled by four genes, each located on a separate chromosome. In the \(\mathrm{F}_{1}\) only round, axial, violet, and full were expressed. In the \(\mathrm{F}_{2},\) all possible combinations of these traits were expressed in ratios consistent with Mendelian inheritance. (a) What conclusion about the inheritance of the traits can be drawn based on the \(\mathrm{F}_{1}\) results? (b) In the \(\mathrm{F}_{2}\) results, which phenotype appeared most frequently? Write a mathematical expression that predicts the probability of occurrence of this phenotype. (c) Which \(\mathrm{F}_{2}\) phenotype is expected to occur least frequently? Write a mathematical expression that predicts this probability. (d) In the \(F_{2}\) generation, how often is either of the \(P_{1}\) phenotypes likely to occur? (e) If the \(F_{1}\) plants were testcrossed, how many different phenotypes would be produced? How does this number compare with the number of different phenotypes in the \(\mathrm{F}_{2}\) generation just discussed?

Albinism, lack of pigmentation in humans, results from an autosomal recessive gene (a). Two parents with normal pigmentation have an albino child. (a) What is the probability that their next child will be albino? (b) What is the probability that their next child will be an albino girl? (c) What is the probability that their next three children will be albino?

Which of Mendel's postulates can only be demonstrated in crosses involving at least two pairs of traits? State the postulate.

Mendel crossed peas having round green seeds with peas having wrinkled yellow seeds. All \(\mathrm{F}_{1}\) plants had seeds that were round and yellow. Predict the results of testcrossing these \(\mathrm{F}_{1}\) plants.

The autosomal (not X-linked) gene for brachydactyly, short fingers, is dominant to normal finger length. Assume that a female with brachydactyly in the heterozygous condition is married to a man with normal fingers. What is the probability that (a) their first child will have brachydactyly? (b) their first two children will have brachydactyly? (c) their first child will be a brachydactylous girl?

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