X-linked recessive disorders are more common in males – why?
Last updated on October 20th, 2022 at 02:12 pm
X-linked recessive disorders are more common in males – why? A Male has one X chromosome and one Y chromosome. The single recessive gene resides on the X chromosome. The Y chromosome doesn’t contain most of the genes on the X chromosome. Because of that, it can’t protect the male from a genetic disorder. Diseases such as haemophilia, and colour blindness occur from a recessive gene on the X chromosome.
X-linked recessive disorders are more common in males – reasons
X and Y chromosomes determine the sex of a human being. Males have one X chromosome and one Y chromosome. And, females have two X chromosomes. The gene of X-linked recessive disorder is passed down on the X chromosome. Since it is passed down on the X chromosome, this type of disorder is more common in men.
X-linked recessive disorders are more common in males. The reason behind this is described below.
The single recessive gene (allele) resides on the X chromosome in case of X-linked recessive disorders. Males have one X chromosome and one Y chromosome. (The Males have only one X chromosome, from their mother.) Now say, the single X chromosome of a male has the recessive disorder allele like haemophilia. The Y chromosome doesn’t contain most of the genes on the X chromosome. Because of that, there is no corresponding allele on their Y chromosome to mask the recessive disorder allele on the X chromosome of a male. Hence the males will have this X-linked recessive disorder.
Females have two X chromosomes, one from their mother and one from their father. As the disorder gene (allele) is recessive, to have the disorder in females both X chromosomes would need to have the gene (allele) responsible for the X-linked recessive disorder, like haemophilia. Hence, this type of disorder is more common in men.
Haemophilia is X linked recessive disorder. The responsible gene is passed down on the X chromosome and the disorder is more common in men. Males have no corresponding allele on their Y chromosome to mask the allele carried on their X chromosome.
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