In: Biology
Hemophilia is a sex-linked recessive trait. Females have two X chromosomes and males have one X chromosome and one Y chromosome. In sex-linked recessive inheritance, one copy of the mutated gene is sufficient to cause the disease to males since they have only one X chromosome. But for females, the two copies of the mutated gene are required to cause the sex-linked recessive disorder. The females with one copy of the mutated gene are carriers. carrier females do not exhibit the trait. In sex-linked inheritance, there is no male to male transmission. The males inherit the X chromosome from the mother and the Y chromosome from the father. the females inherit one X chromosome from the mother and the other X chromosome from the father
Let H be the dominant allele on the X chromosome for normal
Let he be the recessive allele on the X chromosome for hemophilia
Among three children, one is a normal boy (XHY), one is a hemophiliac boy (XhY) and one is a hemophiliac girl (XhXh). The normal boy inherits the normal X chromosome (XH) from the mother and the Y chromosome from the father. The hemophiliac son inherits one copy of the mutated gene (Xh) from the mother and Y chromosome from the father. So the genotype of the mother is XHXh. The mother is a carrier. The hemophiliac daughter inherits one copy of the mutated gene (Xh) from the mother and one copy of the mutated gene (Xh) from the father. So the genotype of the father is XhY. The father is a hemophiliac.
Father has hemophilia (XhY) and the mother is a carrier (XHXh)
Parents : XhY (hemophiliac father) * XHXh (carrier mother)
Gametes of the male parent: Xh, Y
Gametes of the female parent: XH, Xh
Offspring : XHXh (carrier female) , XhXh (hemophiliac female), XHY (normal son), XhY (hemophiliac male)
Therefore, the father is hemophiliac (XhY) and the mother is a carrier (XHXh)