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B
Haemophilia
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C
Colour blindness
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D
Glucose 6-phosphate dehydrogenase deficiency
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Solution
The correct option is Aβ-thalassemia
Colour blindness and hemophilia are X-linked recessive disorder because the governing genes are present on X-chromosome, therefore these diseases are inherited from parent to offspring in sex-linked manner. These disorders are mostly expressed in males because males are hemizygous for chromosome and can express the recessive gene also. Females have two X chromosomes and hence, need two copies of the affected gene to cause the disorder. This means that both disorders are recessive.β-thalassemia is a blood disorder which is caused by the mutation in the Hbb gene present on chromosome 11 and is inherited in an autosomal recessive manner. Glucose-6-phosphate dehydrogenase deficiency is a genetic disorder that causes the destruction of red blood cells is called as hemolysis. It is due to defect in gene present on X-chromosome which codes an enzyme called glucose-6-phosphate dehydrogenase. The correct answer is A.