Tay-Sachs disease is a genetic disorder caused by a mutation in the HEXA gene, resulting in a deficiency of the enzyme hexosaminidase A. It is possible for two healthy individuals to have a daughter with Tay-Sachs disease. Which of the following best describes the inheritance of Tay-Sachs disease?
It is caused by a dominant allele on the X chromosome.
It is caused by a dominant allele on an autosomal chromosome.
It is caused by a recessive allele on an autosomal chromosome.
It is caused by a recessive allele on the Y chromosome.
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