Question

In: Biology

In humans, hypotrichosis (sparse body hair) is a rare autosomal recessive condition. Let h = hypotrichosis...

In humans, hypotrichosis (sparse body hair) is a rare autosomal recessive condition.
Let h = hypotrichosis and H = Normal.
Family A consists of two phenotypically normal parents with five children: the first two have hypotrichosis, and the rest are normal.
Family B consists of a phenotypically normal man and a hypotrichotic woman with three children: one has hypotrichosis, and the other two are normal.
------------
Family C is formed when a normal child from family A marries a normal child from family B.
e.​What is the probability that their first offspring is hypotrichotic?
f.​If they have four children, what is the probability that they will all be normal?

Please answer E and F. Thank you!

Solutions

Expert Solution

Answer:

Family A: Both parents are phenotypically normal. They have normal children and those with hypotrichosis.
This indicates that the recessive allele is present in both the parents, which when passed on to the offsprings will cause the condition to appear.
Therefore family A are phenotypically normal parents and are genotypically heterozygous (Hh). Pedigree is shown here along with probable genotypes.:

Family B: also has hypotrichosis in children. Father is phenotypically normal and his wife has hypotrichosis. Hence genotypically father can only be a heterozygous carrier (Hh). The mother suffers from hypotrichosis hence homozygous recessive (HH). Pedigree is shown here along with genotypes:

Family C: has two phenotypically normal individuals, one from each family A & B. There will be two genotypic possibilities here as shown by two punnet squares (Case I and Case II) below:

Answer e):
The probability that their first offspring is hypotrichotic:

As seen from punnet square above,
In case I - There is a 0% probability, that the first child will be hypotrichotic.
In case II - There is a 25% probability that the first child is hypotrichotic.

Answer f):
The probability that all of their 4 children are normal:

In case I - as seen from the punnet square above, there is a 100% probability, that all 4 children will be normal.

In case II - as seen from punnet square above, the probability can be calculated as -

as one in four children will have hypotrichosis, the chances of a normal child are 3/4 for each child.
Therefore the probability that all four will be normal (without hypotrichosis) will be cumulative
Probability = (3/4) x (3/4) x (3/4) x (3/4) = 81 / 256 = 0.316 OR 31.6% chances that all children will be normal.


Related Solutions

The frequency of carriers for a rare autosomal recessive genetic condition is 0.04 in a population....
The frequency of carriers for a rare autosomal recessive genetic condition is 0.04 in a population. Assuming this population is in Hardy-Weinberg equilibrium, what is the allele frequency of the recessive allele? 0.2 0.4 0.64 0.8 Not enough information is provided.
PKU is a rare, fully penetrant, autosomal recessive condition in which an affected individual cannot break...
PKU is a rare, fully penetrant, autosomal recessive condition in which an affected individual cannot break down the amino acid phenylalanine. Neither Brian nor Mary has PKU, and they want to have children. They are concerned because Brian's father has PKU, and while neither of Mary's parents has PKU, her brother has PKU. Use symbols A and a. 1) What is the probability that Mary and Brian's first child will have PKU? Show work. 2) Mary and Brian have a...
Borishphobia is an autosomal recessive inherited condition in humans that causes AP Biology students to go...
Borishphobia is an autosomal recessive inherited condition in humans that causes AP Biology students to go into convulsions whenever they see the Hardy-Weinberg formula. Complete dominance is the mode of inheritance for the alleles in this condition. In a group of 300 AP Biology students, 97 had convulsions (because they had the condition) during their first Hardy-Weinberg Problem Set. (Assume that students are a representative sample of a population at Hardy-Weinberg equilibrium.) What is the frequency of the borishphobia (b)...
The pedigree from Parts A and B is shown below. Now it shows the inheritance of a rare recessive autosomal condition that affects individuals
The pedigree from Parts A and B is shown below. Now it shows the inheritance of a rare recessive autosomal condition that affects individuals II-3, IV-2, IV-5, and V-3 (denoted by the filled symbols and the genotype aa). Individuals I-1, I-2, I-5, and I-6 have no history of this condition in their families.
Albinism is a rare autosomal recessive trait in which there is a complete absence of melanin...
Albinism is a rare autosomal recessive trait in which there is a complete absence of melanin pigment in the skin, eyes, and hair. A normally pigmented woman whose parents are normal has a brother who is albino. She marries a normally pigmented man whose grandfather was albino. What is the probability their first child will be albino? I would like to see the problem worked out. Dont understand why it is 1/12. Thank you in advance
(1) Haemochromatosis is a mild autosomal recessive condition. Approximately 1 in 200 Australians have the condition,...
(1) Haemochromatosis is a mild autosomal recessive condition. Approximately 1 in 200 Australians have the condition, and approximately 1 in 7 Australians are carriers. Jane is planning on starting a family, and does not have haemochromatosis, though her mother is affected with the condition. Her father is not affected, and is not a carrier. Jane’s partner Steve does not have the condition either, but his father is a carrier (his mother is not a carrier). (a) What are the chances...
In humans, hypercholesterolemia is a dominant autosomal disorder. Color-blindness is a recessive disorder carried on the...
In humans, hypercholesterolemia is a dominant autosomal disorder. Color-blindness is a recessive disorder carried on the X-chromosome. A woman with normal vision who does not have hypercholesterolemia takes her daughter to a doctor for an examination. In the course of the examination, the doctor discovers that the girl is color-blind and has hypercholesterolemia. What does the doctor automatically know about the genotype and phenotype of the girl’s father?
Scalloped (sd) wing is an X-linked recessive and ebony (e) body color is an autosomal recessive...
Scalloped (sd) wing is an X-linked recessive and ebony (e) body color is an autosomal recessive mutation in Drosophila. What proportion of scalloped, ebony colored females is expected in the F2 starting with a true breeding scalloped female which is wild type for ebony mating with a true breeding male mutant only for ebony. a. 1/16 b. 3/16 c. 0 d. 1/8 e. 1/32
1. you are evaluating autosomal recessive condition A (alleles A and a) and B (alleles B...
1. you are evaluating autosomal recessive condition A (alleles A and a) and B (alleles B and b) which you hypothesize are on different chromosomes. You are given 7 wildtype (homozygous dominant) female flies and 7 male flies that are homozygous recessive. What genotypic ratio would you expect in the F1 generation produced? 2. you mate the F1 females with males that are homozygous recessive for both disease A and B to produce an F2 generation. What phenotypic ratio would...
In a population of 16,000 people, 67 are affected with a mild autosomal recessive condition. What...
In a population of 16,000 people, 67 are affected with a mild autosomal recessive condition. What is the estimated number of carriers for this condition in this population?
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT