Psyched101
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I need some help understanding the answer to the following bio genetics question.
A woman is phenotypically normal but had a brother who had an autosomal recessive disorder that resulted in death during infancy. What is the probability that this woman is a carrier of the disorder that afflicted her brother?
a) 1/4
b) 1/3
c) 1/2
d) 2/3
I reasoned that for the brother to have the disease and the woman to be normal both parents had to be heterozygotes (I.e. Aa genotype). This means that there is a 25% chance for homozygous dominant offspring, 50% for heterozygous and 25% homozygous recessive. Since the woman is supposed to be a carrier she falls under the 50% category. Therefore I reasoned the answer is C. But it appears that the answer is D and the justification doesn't explain how they came to that answer.
Thanks in advance for the help!
A woman is phenotypically normal but had a brother who had an autosomal recessive disorder that resulted in death during infancy. What is the probability that this woman is a carrier of the disorder that afflicted her brother?
a) 1/4
b) 1/3
c) 1/2
d) 2/3
I reasoned that for the brother to have the disease and the woman to be normal both parents had to be heterozygotes (I.e. Aa genotype). This means that there is a 25% chance for homozygous dominant offspring, 50% for heterozygous and 25% homozygous recessive. Since the woman is supposed to be a carrier she falls under the 50% category. Therefore I reasoned the answer is C. But it appears that the answer is D and the justification doesn't explain how they came to that answer.
Thanks in advance for the help!