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Masja [62]
3 years ago
11

Why do children with junctional epidermolysis bullosa have fragile skin

Biology
1 answer:
Kazeer [188]3 years ago
4 0
Because of a mutation in the COL7A1 gene which is the gene that provides the body with instructions for making the protein that form the pieces of a larger protein that makes collagen
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Read 2 more answers
Galactosemia is a recessive human disease that is treatable by restricting lactose and glucose in the diet. Susan Smithers and h
lord [1]

Answer:

a. 81/256

b. 175/256

C. 1/4

D. 9/256

E. 54/256

Explanation:

Since both parents are heterozygous for galactosemia (Gg). The possibility of their children will be

GG Gg Gg gg. The probability for one child to be unaffected is 3/4 and affected is 1/4 since it is a recessive diseases:

A. Probability for none of the four children to be affected is 3/4*3/4*3/4*3/4=81/256

B.

Since the probability of unaffected children is 81/256

The probability that at least one child will be affected is 1-(3/4*3/4*3/4*3/4)=1-(81/256)

= 175/256

C. The probability that only one if the child will be affected is 1/4

D. The probability that the first two will have galactosemia and the second two will not is

1/4*1/4*3/4*3/4=9/256

E. The probability that two will have galactosemia and two will not, regardless of order.

Since the probability that two will have galactosemia and two will not is 9/256.

The total possible outcome that 2 among 4 children will be born regardless of order (first and second, first and third, first and fifth, second and third, second and fourth, third and fourth) is 6

Hence the probability two will have galactosemia and two will not, regardless of order is 9/256*6= 54/256

7 0
3 years ago
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