The mother has a 50% chance of passing the defective recessive gene to her daughters who will be carries of the disorder (like their mother).
The son would automatically get the Y chromosome from the father. The son's X chromosome has to come from his mother. Females are XX, so he has a fifty-fifty chance of receiving the disease carrying gene. If he receives the disease carrying gene he will have the disease, if he doesn't then he will neither have the disease nor be a carrier. A daughter has to receive one X chromosome from her father and one from her mother. If the father doesn't have the disease, then the daughter cannot have it. If the mother is a carrier, then she has a fifty-fifty chance of being a carrier.
The son would automatically get the Y chromosome from the father. The son's X chromosome has to come from his mother. Females are XX, so he has a fifty-fifty chance of receiving the disease carrying gene. If he receives the disease carrying gene he will have the disease, if he doesn't then he will neither have the disease nor be a carrier. A daughter has to receive one X chromosome from her father and one from her mother. If the father doesn't have the disease, then the daughter cannot have it. If the mother is a carrier, then she has a fifty-fifty chance of being a carrier.
The problem with genetic diseases is that they are never gone. Say bob has the hemophelia desease and his wife is a carrier of the disease as well. Their children have a one in two chance of having the disease or being carriers because the disease is recessive. Now if bob's wife was not a carrier, their children would have a one in one chance of being a carrier. The problem is the disease is spread by the carriers.
Hemophilia almost always affects boys. Why? Because the disease is an X-linked genetic disorder, passed from mother to son. Boys get an X chromosome (say: kro-muh-soam) from their mother and a Y chromosome from their father. If the mother carries the gene for hemophilia on one of her X chromosomes (girls have two X chromosomes), each of her sons will have a 50% chance of having hemophilia.A mother who is a carrier also has a 50% chance of giving the faulty X chromosome to her daughter. That does not give the daughter the hemophilia disease, but it does result in the daughter becoming a hemophilia carrier. So it's possible one of her sons someday could have the disease.
Bipolar Disorder is not a disease - you cannot catch it or carry it or give it to someone else. There does seem to be a genetic trait that you inherit, so that if your ancestors were bipolar, you will have a bigger chance of having it yourself, but it is a chance and not a certainty.
No, this is an inherited disease. If you are concerned about having a child with cf you can get genetic testing to see if you and your partner are carriers of the gene. If you and your partner are carriers - 25% chance If one of you has CF and the other is a carrier - 50% chance If you both have CF - baby will have CF If neither partner is a carrier - 0% chance
No, this is an inherited disease. If you are concerned about having a child with cf you can get genetic testing to see if you and your partner are carriers of the gene. If you and your partner are carriers - 25% chance If one of you has CF and the other is a carrier - 50% chance If you both have CF - baby will have CF If neither partner is a carrier - 0% chance
Refsum disease is inherited as an autosomal recessive disorder, which means that two unaffected carrier parents have a 25% chance of having an affected child in every pregnancy.
First of all why is this in Justin Bieber? Anyways, yes, it is possible for a girl to have ALD. Originally the disease only affected boys, but because of new treatments these boys are living into puberty. This means that they could possibly impregnate a female carrier of ALD. If they were to have a daughter, then their daughter would have a 50% chance of having ALD.
No. The trait that causes sickle cell anemia is a recessive trait, which means that if both parents have the trait, there is a 1/4 chance their child will have it. The child can be a carrier however and not display symptoms, but there is no way for a child to get sickle cell from parents that don't have the gene.
By definition, Y-linked diseases cannot pass to a daughter. X-linked diseases can, but many of them are mitigated or eliminated if the X from the mother does not possess the defect, in which case your daughter would be a carrier, and her sons would have a 50/50 chance of inheriting the disease.
There are no hard answers to this, it depends strictly on luck. The statistics are though not very good for their children. Statisically the couple have a chance of having a normal son, a daughter that is a carrier for hemophilia, a daughter with hemophilia and a son with hemophia.