A family that exhibits Fragile X syndrome is shown in the pedigree. In the pedigree, squares represent males and circles represent females. Shaded symbols represent a person with the disorder.   Which of the following correctly predicts the outcome if offspring 11 mated with a homozygous normal female, based on the inheritance pattern shown in the pedigree? The male offspring would exhibit Fragile X syndrome because Fragile X is an X-linked recessive trait. The female offspring would exhibit Fragile X syndrome because Fragile X is a recessive autosomal trait. None of their offspring would exhibit Fragile X syndrome because Fragile X is an X-linked dominant trait.

Human Heredity: Principles and Issues (MindTap Course List)
11th Edition
ISBN:9781305251052
Author:Michael Cummings
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Chapter15: Genomes And Genomics
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Fragile X syndrome, caused by a change in the FMR1 gene, is the most common form of intellectual disability. In patients with this syndrome, a small part of the gene is repeated several times in one area of the chromosome. This defect in the gene makes the body unable to produce adequate amounts of a protein needed for normal brain functioning. In males, this syndrome causes a moderate intellectual disability, and in females, a mild intellectual disability.

A family that exhibits Fragile X syndrome is shown in the pedigree. In the pedigree, squares represent males and circles represent females. Shaded symbols represent a person with the disorder.

 

Which of the following correctly predicts the outcome if offspring 11 mated with a homozygous normal female, based on the inheritance pattern shown in the pedigree?

The male offspring would exhibit Fragile X syndrome because Fragile X is an X-linked recessive trait.
The female offspring would exhibit Fragile X syndrome because Fragile X is a recessive autosomal trait.
None of their offspring would exhibit Fragile X syndrome because Fragile X is an X-linked dominant trait.
Both the male and female offspring exhibit Fragile X syndrome because Fragile X is a dominant autosomal trait.
 
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