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Suppose that a disease is inherited via a dominant mode of inheritance and that only one of the two parents is affected with the disease. The implications of this mode of inheritance are that the probability is 1 in 2 that any particular offspring will get the disease.Suppose the older child is affected. What is the probability that the younger child is affected?

Short Answer

Expert verified
The probability that the younger child is affected is 1/2 or 50%.

Step by step solution

01

Understanding Dominant Inheritance

In a dominant mode of inheritance, only one parent needs to have the dominant allele for a disease trait to potentially appear in the offspring. If a parent is affected by a dominant disease, they can either pass the dominant affected allele (D) or the normal recessive allele (d) to any child. Hence each child has a 50% chance of inheriting the dominant disease allele.
02

Probability of Each Child

Given that the parent is affected, each child has a 1 in 2 probability (or 50% chance) of inheriting the disease. This probability is independent for each child, meaning the inheritance of the dominant allele by one child does not affect the probability for the other child.
03

Independence of Events

The event that the older child is affected is independent of the genetic outcome for the younger child. In probability, two independent events occurring do not change the likelihood of one another. Therefore, the genetic condition of one sibling does not impact the probability for the other sibling.
04

Calculating the Required Probability

Since each child's genetic outcome is independent, and given that the probability for any child to inherit the disease remains 1 in 2, the probability that the younger child is affected is simply the same as it was calculated independently of the older child’s condition.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Dominant Inheritance
Dominant inheritance is a fundamental genetic concept that explains how certain traits or diseases are passed from parents to offspring. In simple terms, it involves the presence of a dominant allele, which is the genetic code that can overpower a recessive counterpart. When a trait or disease is inherited dominantly, only one affected parent needs to pass on the dominant allele for the trait or disease to manifest in the child.

Consider a scenario where one parent has a dominant allele for a specific trait, denoted by "D". The other allele, which is recessive, is denoted by "d". This parent has a pair of alleles like this: (D, d). Any child of this parent has a 50% chance of inheriting the dominant allele "D", simply because the parent will randomly transmit either "D" or "d" with equal likelihood.

  • Dominant alleles cause the trait to appear even when only one is present.
  • Recessive alleles require two copies to express the trait.
Understanding this basic principle of genetics can help in predicting the likelihood of a child having a certain trait, especially when considering diseases that follow dominant inheritance patterns.
Probability Theory
Probability theory is a branch of mathematics concerned with analyzing random events. In the context of genetic inheritance, it helps us quantify the chances or likelihood of passing certain traits or diseases from parents to children.

When considering the likelihood of offspring inheriting a genetic trait, probability offers a numerical perspective. For a trait following dominant inheritance and if one parent is affected, each child's probability of inheriting the trait can be calculated using basic probability principles. With a 1 in 2 chance, we can say the probability is 0.5 or 50%.

Important basics in probability include:
  • Probability values range from 0 to 1, where 0 signifies impossibility and 1 indicates certainty.
  • The probability of independent events, like genetic transmission to different offspring, doesn't influence each other's outcomes.
By applying these principles, one can calculate and understand how genetic traits may be passed on within families.
Independent Events
In probability, independent events are those where the occurrence of one event does not affect the occurrence of another. This concept is crucial in understanding genetic inheritance, particularly in scenarios where multiple children inherit traits from their parents.

When we say the inheritance traits of siblings are independent, it means that the genetic outcome for one child does not influence the genetic outcome for another sibling. In our example of a disease inherited dominantly, the chance of one child being affected is independent of whether their sibling is affected or not.

Consider:
  • The probability remains 50% for each child, regardless of their sibling's genetic outcome.
  • Each child's genetic inheritance is a separate event.
This principle helps genetic counselors and families understand that the condition of one sibling offers no predictive insight into the condition of another sibling when the events are independent.

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Most popular questions from this chapter

Consider a family with a mother, father, and two children. Let \(A_{1}=\left\\{\text { mother has influenzal, } A_{2}=\\{ \text { father has influenzal, }\right.\) \(A_{3}=\left\\{\text { first child has influenzal, } A_{4}=\\{ \text { second child has influ- }\right.\) enzal, \(B=\) lat least one child has influenzal, \(C=\) lat least one parent has influenzal, and \(D=\\{\) at least one person in the family has influenzal.What does \(A_{1} \cup A_{2}\) mean?

Suppose that a disease is inherited via a dominant mode of inheritance and that only one of the two parents is affected with the disease. The implications of this mode of inheritance are that the probability is 1 in 2 that any particular offspring will get the disease. If \(A, B\) are two events such that \(A=\\{\) older child is affected \(\\}, B=\\{y \text { ounger child is affected }\\}\), then are the events \(A, B\) independent?

The familial aggregation of respiratory disease is a wellestablished clinical phenomenon. However, whether this aggregation is due to genetic or environmental factors or both is somewhat controversial. An investigator wishes to study a particular environmental factor, namely the relationship of cigarette-smoking habits in the parents to the presence or absence of asthma in their oldest child age 5 to 9 years living in the household (referred to below as their offspring). Suppose the investigator finds that (1) if both the mother and father are current smokers, then the probability of their offspring having asthma is \(.15 ;(2)\) if the mother is a current smoker and the father is not, then the probability of their offspring having asthma is \(.13 ;(3)\) if the father is a current smoker and the mother is not, then the probability of their offspring having asthma is \(.05 ;\) and (4) if neither parent is a current smoker, then the probability of their offspring having asthma is .04.Suppose the smoking habits of the parents are independent and the probability that the mother is a current smoker is \(.4,\) whereas the probability that the father is a current smoker is .5. What is the probability that both the father and mother are current smokers?

A dominantly inherited genetic disease is identified over several generations of a large family. However, about half the families have dominant disease with complete penetrance, whereby if a parent is affected there is a \(50 \%\) probability that any one offspring will be affected. Similarly, about half the families have dominant disease with reduced penetrance, whereby if a parent is affected there is a \(25 \%\) probability that any one offspring will be affected. Suppose in a particular family one parent and two of the two offspring are affected.What is the probability that the mode of transmission for this particular family is dominant with complete penetrance? Is this a prior probability or a posterior probability?

Suppose that a disease is inherited via a sex-linked mode of inheritance. The implications of this mode of inheritance are that each male offspring has a \(50 \%\) chance of inheriting the disease, whereas the female offspring have no chance of getting the disease.In a family with one male and one female sibling, what is the probability that both siblings are affected?

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