Question

. A man’s grandfather has galactosemia, a rare autosomal recessive disease caused by the inability to...

. A man’s grandfather has galactosemia, a rare autosomal recessive disease caused by the inability to process galactose, leading to muscle, nerve, and kidney malfunction. The man married a woman whose sister had galactosemia. The woman is now pregnant with their first child.

b. What is the probability that this child will have galactosemia?

c. If the first child does have galactosemia, what is the probability that a second child will have it?

Homework Answers

Answer #1

The probability of the man getting the defected allele is 1/4

1/2 probability of the child being a male and another 1/2 for him to acquire the disease allele

The woman must be atleasr a carrier if her sister suffered from the disease i.e. the probability of her having the allele is 1/2

The probability For both these to produce a child with the disease is 1/4*1/2=1/8

C. The probability of the disease occurrence will remain the same irrespective of the order and sex.

Know the answer?
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for?
Ask your own homework help question
Similar Questions
In humans, the disease galactosemia is inherited as a rare autosomal recessive trait in a simple...
In humans, the disease galactosemia is inherited as a rare autosomal recessive trait in a simple Mendelian manner. A normal woman whose father had galactosemia intends to marry a normal man whose grandfather had galactosemia. What is the probability that their first child will have galactosemia? A. 1/2 B. 1/8 C. 1/16 D. 1/4 E. 0 Correct Answer: B. 1/8 Can you explain why?
The disease galactosemia is an autosomal recessive trait. A man whose sister had galactosemia intends to...
The disease galactosemia is an autosomal recessive trait. A man whose sister had galactosemia intends to start a family with a woman whose great-grandfather was galactosemic. They are worried about having a galactosemic child. (assume no other relatives brought galactosemia-causing variants into the family) What is the probability of their first child being affected with the condition?
Polycystic disease (PKD)is an autosomal dominant disease. Symptoms of the disease do not usually present until...
Polycystic disease (PKD)is an autosomal dominant disease. Symptoms of the disease do not usually present until age 40-50, but it can now be diagnosed earlier using genetic testing. A woman, whose mother died of PKD, marries a man wo has no history of PKD in his family. The woman is pregnant with their third child. Their first child, a boy, has PKD. Their second child, a daughter, does not. What are the chances that this child will have PKD?
Sickle cell anemia is an autosomal recessive disease. A man and a woman are both heterozygous...
Sickle cell anemia is an autosomal recessive disease. A man and a woman are both heterozygous for the mutant gene. They have two children and one has the disease. What are the chances their next child will have the disease? 100% 75% 50% 25%
Lesch-nyhan syndrome is an x-linked, rare, recessive disease caused by a mutation in the gene encoding...
Lesch-nyhan syndrome is an x-linked, rare, recessive disease caused by a mutation in the gene encoding for hypoxanthine-guanine phosphoribosyltransferase (HPRT1). A woman’s maternal grandfather suffered from lesch-nyhan syndrome. She is concerned her male child could have lesch-nyhan syndrome. Genetically, what is the chance that this child has lesch-nyhan syndrome? a.) 0 b.) 1/8 c.) 1/4 d.) 1/16 e.) 1/2
Seborrheic keratosis is a rare hereditary skin condition caused by an autosomal dominant mutation. Affected people...
Seborrheic keratosis is a rare hereditary skin condition caused by an autosomal dominant mutation. Affected people have skin marked with a number of small, sharply margined, yellowish or brownish areas covered with a thin, greasy scale. An affected man, whose father also had keratosis but whose mother did not, marries a normal woman and they have four children. A) What is the chance that all four are normal? B) What is the chance that at least two of the four...
Two cousins marry and their first child has a rare autosomal recessive trait conferring high musical...
Two cousins marry and their first child has a rare autosomal recessive trait conferring high musical ability. If they plan to have 6 children, compute the expected chance that exactly four of the six children will inherit this trait. Please show me how you got it so I can understand. Also is the chance that they inherit this trait referring to them being homozygous recessive or heterozygous?
Dentinogenesis imperfecta is a tooth disorder. The trait is inherited as an autosomal dominant allele in...
Dentinogenesis imperfecta is a tooth disorder. The trait is inherited as an autosomal dominant allele in humans. Assume that a male with dentinogenesis imperfecta, whose mother had normal teeth, married a woman with normal teeth. They had four children. What is the probability that their first child will be a male with dentinogenesis imperfecta? What is the probability that three of their four children will have the disease?
Cystic fibrosis is a genetic disease caused by several variants of a gene. It is autosomal...
Cystic fibrosis is a genetic disease caused by several variants of a gene. It is autosomal recessive. In other words, an individual must receive two copies of a cystic fibrosis genetic variant, one from the father and one from the mother, to manifest the condition. The probability that a child will be born with cystic fibrosis in the US is about 0.0004. a. Assuming independent inheritance from the father and mother, what is the probability that any given copy of...
You are working as a genetic counsellor. A newly married couple comes to you for advice....
You are working as a genetic counsellor. A newly married couple comes to you for advice. Neither the man nor the woman has cystic fibrosis, but both have full siblings with this genetic disease. Cystic fibrosis is an autosomal recessive disease caused by a single locus and is typically diagnosed by the time a child is 2 years old. The young couple are planning to start a family and are worried about the risk that they might conceive a child...