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Author11 Posts
  #1

A 30-year-old man has a sister who died from infantile Tay-Sachs disease, an autosomal recessive disorder that is lethal by age 6. What is the probability that this man is a heterozygous carrier, and, if 1% of individuals in the general population are heterozygous carriers, what is the probability that this man will produce an affected offspring if he mates with a member of the general population?

  #2

0.0025

  #3

1st part of the question=the person may have 2/3 rd chance of being a carrier of the disease if we consider that his parents were both heterozygous for the disease(as is commonly seen).
2nd part---chances of his child being affected by the disease if he happens to be carrier(considering his wife a carrier too)=2/3x1/100x.25=0.0017

  #4

anne,
How did you know 2/3 chance of being a carrier ?

Its 25 % right (for AR diseases)

  #5

as its an AR condition,and we suppose(as in most cases)that his parents would both be carriers,the person has 1/4th chance of being affected,and 3/4th chance of being unaffected.if the person is unaffected,he has 1/3rd chance of being homozygous normal,and 2/3rd chance of being a carrier.

  #6

good q smiling face

  #7

can you please explain how you calculated che chance of the woman being heterozygote, since the offspring will only be affected if the man mates with a heterozygote female.

___________________
if you haven't any charity in your heart, you have the worst kind of heart trouble.

  #8

as 1% of the individuals in the population are heterozygous,we calculate it by guessing that the woman may be a carrier.

  #9

thanks anne

  #10

i will like to know one think. i thought the hardy weiberg rule would have been applied. had it been the prevalence of the heterozygote was 10% or 5%, would we have assumed that the lady is eterozygote?

___________________
if you haven't any charity in your heart, you have the worst kind of heart trouble.

  #11

i still didnt get the calculation part ...plz explain ...









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