HELP PLEASE I LUV YALL A child is born with cystic fibrosis, an inherited recessive disorder. No one in the family (on either side) for several generations is known to carry the gene or have the disorder. How can this be explained?
a The genetic disorder formed from the mother's poor nutrition and prenatal care.
b There was a mutation in the DNA, either in one of the gametes or the fertilized egg.
c The child contracted the illness from another child when he was born.
d The child developed the disorder when he was born; it is a result of a birth defect.

i looked it up and i think its A correct me if i am wrong

Explanation:

the answer is in bold btw

its either B or D because it didn't directly state anything about the father, and it also says it was inherent so it wouldn't be contracted, so that eliminates A and C, so mutations don't actually happen in babies/cubs ect, they actually happen months after birth, and slowly begin growing themselves in, so it will be answer D, The child developed a birth defect

drfgt dfs f grftsrh fg rts gh   htr hr rs t

answer: i cant find your answer. do u have another way i can answer it for you : )

explanation: