Huntington's Disease: Risk of Inheritance in Early 20s

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A man in his early twenties learns his father has Huntington's Disease, which is caused by a dominant allele. Since his mother does not carry the allele, the father's genotype is Hh, while the mother's is hh. The probability of the son inheriting the dominant allele and developing the disease later in life is 50%. This is determined through a Punnett square analysis, showing equal chances of the son being either Hh (affected) or hh (normal). Understanding these genetic probabilities is crucial for assessing the risk of inheritance.
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A man in his early twenties who is normal learns that his father has developed Huntington's Disease, a rare, fatal disease caused by a dominant allele, which usually manifests itself in middle age (since the disease is rare, it is safe to assume that he is heterozygous). What is the probability that the younger man wil also develop the symptons later in life? (His mother does not carry a dominant allele.)
 
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To get you started: what do you think the genotypes are of the young man's father and mother with respect to the gene discussed?
 
It is a literal 50% chance of developing the disease. Let's say H represents the allele for Huntington's.. and h represents normal. Then the father would be Hh, and the mother would be hh. Then in having a child, there is a 50% chance of the child being Hh, 50% chance of the child being hh. (we can determine this probability using a punnett square)
 
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