Achondroplasia (dwarfism) is an example of a dominantly inherited disease. Individuals who have the dominant gene (A) have the dwarfism phenotype, while normal height is recessive (a). What is the probability of having children with achondroplasia between a normal height female and a heterozygote achondroplasia male?

Human Anatomy & Physiology (11th Edition)
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问题13
Achondroplasia (dwarfism) is an example of a dominantly inherited disease. Individuals who have the
dominant gene (A) have the dwarfism phenotype, while normal height is recessive (a). What is the
probability of having children with achondroplasia between a normal height female and a
heterozygote achondroplasia male?
100%
75%
25%
50%
Transcribed Image Text:问题13 Achondroplasia (dwarfism) is an example of a dominantly inherited disease. Individuals who have the dominant gene (A) have the dwarfism phenotype, while normal height is recessive (a). What is the probability of having children with achondroplasia between a normal height female and a heterozygote achondroplasia male? 100% 75% 25% 50%
Expert Solution
Step 1: Achnodroplasia

Achondroplasia or dwarfism is a genetic bone disorder affecting one in 20,000 babies. It is the most prevalent kind of dwarfism. The head is generally large, but the trunk is average in size. The child's arms and legs are short in comparison to the body length. Adult girls with achondroplasia have an average height of 49 inches (or 4 feet 1 inch) and adult males with achondroplasia have an average height of 52 inches (or 4 feet 4 inches). 

The most common symptoms of achondroplasia are normal intelligence, curved lower spine, small vertebral canal, misaligned teeth, poor muscle tone, loose joints, flat feet, etc.

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