Chapter 12: Problem 8
Color blindness is a case of________ inheritance. a. autosomal dominant b. autosomal recessive c. X-linked dominant d. X-linked recessive
Short Answer
Expert verified
Color blindness is an X-linked recessive inheritance.
Step by step solution
01
Understand the Question
The exercise asks us to identify the type of genetic inheritance that color blindness represents. We have four options: autosomal dominant, autosomal recessive, X-linked dominant, and X-linked recessive.
02
Identify Type of Color Blindness
Color blindness is primarily considered a genetic condition that affects the ability to perceive colors correctly. It is most commonly inherited as an X-linked recessive trait.
03
Explanation of X-linked Recessive Inheritance
X-linked recessive means the gene causing the trait or disorder is located on the X chromosome. For males (XY), inheriting one affected X chromosome will result in color blindness. For females (XX), both X chromosomes must be affected for the condition to manifest, making it less common in females than in males.
04
Evaluation of Options
Compare the description of color blindness inheritance (X-linked recessive) with the given options: a) autosomal dominant, b) autosomal recessive, c) X-linked dominant, d) X-linked recessive. The correct matching type of inheritance is 'X-linked recessive' (option d).
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Key Concepts
These are the key concepts you need to understand to accurately answer the question.
Color Blindness
Color blindness is a condition that affects an individual's ability to distinguish certain colors. This can make it hard for people to perceive the full color spectrum.
- Red-green color blindness is the most common type, followed by blue-yellow and complete color blindness.
- The condition arises from issues with the photopigments in the eyes.
- Color blindness is commonly diagnosed through visual tests.
X-linked Recessive Inheritance
X-linked recessive inheritance is a type of inheritance where the gene causing the trait is present on the X chromosome. Here's how it works:
- Males have one X and one Y chromosome (XY). Having one affected X chromosome means the trait or disorder will present, as there is no second X chromosome to mask the effect of the recessive gene.
- Females have two X chromosomes (XX). In this case, both X chromosomes must have the recessive gene for the trait to manifest.
Autosomal Dominant
Autosomal dominant inheritance involves genes located on non-sex chromosomes, known as autosomes.
- In this type of inheritance, only one copy of a mutated gene, from either parent, is sufficient to cause the disorder.
- Both males and females are equally likely to inherit autosomal dominant traits because it is not linked to sex chromosomes.
- Conditions with this inheritance pattern can occur in every generation of a family.
Autosomal Recessive
Autosomal recessive inheritance also involves genes on the autosomes but requires two copies of the mutated gene to present the disorder.
- Individuals receive one recessive gene from each parent to express the trait.
- Carriers, with only one recessive gene, don't typically show symptoms.
- It affects males and females equally across generations.