Likelihood of inheriting autosomal dominant diseases

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In summary, the probability of inheriting the gene for Huntington's disease from a parent with the disease is not a simple 50%, but rather depends on the proportion of heterozygotes in the population, which is likely to be much higher than the proportion of homozygotes.
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Qube
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If one of your parents has Huntington's disease, you have a 50% chance of getting the gene for the disease.

This IS wrong. This only holds true if one of your parents is HETEROZYGOUS dominant.

Hh x hh => 50% chance of offspring having Huntington's disease.

However, if one of your parents is HOMOZYGOUS DOMINANT ..

HH x hh => 100% chance of offspring having Huntington's diseases.

Simple Punnett squares will verify the above.

Therefore, the probability should be 75% if one parent has Huntington's disease. Am I right?
 
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  • #2
Qube said:
This IS wrong. This only holds true if one of your parents is HETEROZYGOUS dominant.

Hh x hh => 50% chance of offspring having Huntington's disease.

However, if one of your parents is HOMOZYGOUS DOMINANT ..

HH x hh => 100% chance of offspring having Huntington's diseases.

Simple Punnett squares will verify the above.

Therefore, the probability should be 75% if one parent has Huntington's disease. Am I right?

I don't know what you are quoting or context, but I'd guess this is an approximation based on homozygous being rare in the population.

The dynamics of Huntingdon's is a bit more complex than just the inheritance of a stable chromosome, and was explained in a recent thread on PF.
 
  • #3
You are making the faulty assumption that heterozygotes and homozygotes are equally abundant. In reality, the probability is 0.5p+(1-p), where p is the proportion of Huntington's patients who are heterozygous for the disease allele. As mentioned by epenguin, the disease allele is rare, so there are many more heterozygotes than homozygotes, and p~1.
 

1. What is an autosomal dominant disease?

An autosomal dominant disease is a genetic disorder caused by a mutation in one copy of a gene on one of the 22 non-sex chromosomes (known as autosomes). This means that a person only needs to inherit one copy of the mutated gene from either parent to develop the disease.

2. How likely is it to inherit an autosomal dominant disease?

The likelihood of inheriting an autosomal dominant disease depends on whether or not a parent has the mutated gene. If a parent has the mutated gene, there is a 50% chance that they will pass it on to their child. If neither parent has the mutated gene, the likelihood of inheriting the disease is very low.

3. What are some examples of autosomal dominant diseases?

Some examples of autosomal dominant diseases include Huntington's disease, Marfan syndrome, and polycystic kidney disease. These diseases vary in their severity and symptoms, but all are caused by a mutation in a single gene on an autosome.

4. Are there any treatments for autosomal dominant diseases?

Currently, there are no cures for autosomal dominant diseases. However, there are treatments available that can help manage symptoms and improve quality of life. These treatments may include medications, lifestyle changes, and supportive therapies.

5. Can autosomal dominant diseases be prevented?

In most cases, it is not possible to prevent the development of an autosomal dominant disease if a person has inherited the mutated gene. However, genetic testing can help identify individuals who are at risk for inheriting these diseases, allowing for early detection and management.

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