Duchenne muscular dystrophy is inherited in which pattern?

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Multiple Choice

Duchenne muscular dystrophy is inherited in which pattern?

Explanation:
X-linked recessive inheritance explains Duchenne muscular dystrophy. The dystrophin gene is on the X chromosome, so males, with only one X, develop the disease if that X carries the mutation. Females have two X chromosomes, so one mutated copy usually makes them carriers and often asymptomatic due to protective effects from the second X. An affected male passes the mutated X to all daughters (who become carriers) and to none of his sons, while a carrier mother has a 50% chance with each pregnancy to have a son who is affected and a daughter who is a carrier. This pattern accounts for the strong male predominance and the absence of father-to-son transmission. The other inheritance patterns don’t fit this usual family pattern.

X-linked recessive inheritance explains Duchenne muscular dystrophy. The dystrophin gene is on the X chromosome, so males, with only one X, develop the disease if that X carries the mutation. Females have two X chromosomes, so one mutated copy usually makes them carriers and often asymptomatic due to protective effects from the second X. An affected male passes the mutated X to all daughters (who become carriers) and to none of his sons, while a carrier mother has a 50% chance with each pregnancy to have a son who is affected and a daughter who is a carrier. This pattern accounts for the strong male predominance and the absence of father-to-son transmission. The other inheritance patterns don’t fit this usual family pattern.

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