The reason why X-linked recessive allele of muscular dystrophy may be present in the family of the employee which affected his son. Introduction: X-linked recessive alleles are expressed in homozygous individuals. Mother can be a carrier of the mutated X-linked recessive allele because she is heterozygous for the condition and did not develop any diseased condition.

Question

In man, muscular dystrophy is a condition in which the muscles waste away during early life and may result in a shorter life expectancy. It is due to a sex-linked, recessive gene. A certain couple has five children – three boys (ages 1yr, 3yrs, and 10yrs old) and two girls (ages 5yrs and 7yrs old). The oldest boy shows the symptoms of this disease. You are their family physician and they come to you for advice. What would you tell them about the chances of their other children developing the disease?

Answer 1

Question

Chapter 11, Problem 7QP

Summary Introduction

To explain: The reason why X-linked recessive allele of muscular dystrophy may be present in the family of the employee which affected his son.

Introduction: X-linked recessive alleles are expressed in homozygous individuals. Mother can be a carrier of the mutated X-linked recessive allele because she is heterozygous for the condition and did not develop any diseased condition.

Expert Solution & Answer

Trending nowThis is a popular solution!

See solution

Check out sample textbook solution

Students have asked these similar questions

In man, muscular dystrophy is a condition in which the muscles waste away during early life and may result in a shorter life expectancy. It is due to a sex-linked, recessive gene. A certain couple has five children – three boys (ages 1yr, 3yrs, and 10yrs old) and two girls (ages 5yrs and 7yrs old). The oldest boy shows the symptoms of this disease. You are their family physician and they come to you for advice. What would you tell them about the chances of their other children developing the disease?

Lauren has chronic bronchitis and frequently ends up hospitalized with pneumonia. She has no family history of cystic fibrosis, a serious recessive genetic disorder which affects respiratory and digestive tracts. She and her husband Nat have one child after undergoing fertility treatments to overcome Nat's infertility. They are surprised when their child is diagnosed with cystic fibrosis and the genetic counselor tells them that they each also have the condition, which causes their bronchitis and infertility. Which of the following would be a reasonable explanation of their situation? Although the underlying disease is genetic, the severity of the disorder if influenced by environmental variation. Cystic fibrosis displays variable expressivity. There are different alleles of cystic fibrosis which cause differing forms of the disease. There are different alleles of cystic fibrosis which cause differing forms of the disease and Cystic fibrosis displays variable expressivity are the only…

A woman knows that her mother is a carrier of Kartagener’s syndrome (an autosomal recessive disorder). The woman does not know if either she or her husband are carriers. The couple wants to have a child, but is worried about whether or not they could have a child with Kartagener’s syndrome. Should the couple seek the advice of a genetic counselor? In other words, is there a chance they could have an affected child? If there is a chance, please make sure your answer includes the specific parental genotypes necessary to make this possible.