Females who are carriers of hemophilia possess one normal and one mutated allele of the gene responsible for the disorder, typically located on the X chromosome. While they often do not exhibit severe symptoms of hemophilia due to the presence of the normal allele, they can experience mild bleeding problems and have a 50% chance of passing the mutated allele to their offspring. Male children who inherit the mutated allele will be affected by hemophilia, while female children may become carriers themselves. Genetic counseling is recommended for carriers to understand the risks for future generations.
XhXh - with hemophilia XhXH- carrier of hemophilia
Yes females can have hemophilia. Although very rare it has been recorded. A female can get hemophilia if her mother is a carrier and her father has it. Like I said, It doesn't happen often but is possible.
hemophilia is a recessive gene, if you are A female that is a carrier then if you were to have a male child it will be passed on to him. As well as if you were to have a male child who would have hemophilia. your daughter would need to be tested to see if she carried it as well. Only Males have hemophilia but females carry it.My family has dealt with hemophilia for years.My great Aunt carrier, her son has hemophiliaMy mother a carrier, my brother has hemophilia, I do not carry it.My Aunt is a carrier, my cousin he has it, his sister carrier as well.The scientific answer isThis is due to the fact that females have two X chromosomes while males have only one, lacking a 'back up' copy for the defective gene the defective gene becomes manifest more easily in males. Because females have two X chromosomes and because haemophilia is rare, the chance of a female having two defective copies of the gene is very low, thus females are almost exclusively asymptomatic carriers of the disorder.
You would get it from your mother. It is a sex-liked genetic disorder. Females are the carriers, males exhibit the condition.
A carrier for hemophilia is a female who carries the genetic mutation for hemophilia on one of her X chromosomes, but does not exhibit symptoms of the condition herself. Carriers can pass on the gene mutation to their children, resulting in hemophilia in male offspring. Testing can confirm carrier status.
Hemophilia normally refers to a genetic disorder that can be either inherited or the result of a spontaneous mutation. Since the genetic form of hemophilia is linked to a mutation on the X chromosome, males typically show the full symptoms while females with the mutation typically have somewhat mitigated symptoms or none at all. While the majority of the cases of genetic hemophilia are inherited, meaning that the genes were passed down from the the parents, approximately 1/3 of the cases are spontaneous mutations. The mutation occurs at conception, meaning that all genetic forms basically take effect at birth. Acquired hemophilia is a result of some other influence such as liver damage or specific medications. This form of hemophilia is neither inherited nor genetic. In short, technically anyone can get hemophilia. Genetic hemophilia is present at birth, and it tends to impact the health of males more than females, but can affect females too.
Her father has to have hemophilia as well, and the mother is a carrier or also has hemophilia. So if we pretend that the hemophilia gene is "x", you need to have "xx" to have hemophilia. The father must have the genotype "Yx" and the mother has the have "Xx" or "xx".
50
50
Anyone can inherit hemophilia. In most cases, it is a man whose mother is a carrier of the disease. It is extremely rare for a woman to have hemophilia but it is not uncommon for one to be a carrier. It is even possible for someone whose family has no record of hemophilia to get it through gene mutations.
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.
females have 2 alleles for hemophilia, (X^hX^H) and (X^hX^h) if H is the normal allele and h is the recessive allele for hemophilia