Is Hemophilia Genetic?

Hemophilia is a disorder in the genes of any individual. To answer is hemophilia genetic, one has to understand the two ways through which the disease can be acquired: Either by inheritance Or by a de novo mutation of the genes. Is hemophilia genetic and its genetic significance can also be ascertained by its hereditary nature. Humans have 23 pairs of chromosomes. Out of which, one pair of chromosome is responsible for determining the sex of an individual, these are called sex chromosomes. While men have a combination of XY chromosomes, females are XX. Patients suffering from hemophilia... Read More

Hemophilia Definition, Causes, and Treatment

The word hemophilia definition literally means “lover of blood”. That human have 23 pairs of chromosomes. Out of which one pair of chromosome is responsible for determining the sex of an individual, these are called sex chromosomes. While men have a combination of XY chromosomes, females are XX. Patients suffering from Hemophilia have a faulty X- chromosome this can be inherited from either parents or can be the caused due a new mutation. The haemophilic X chromosome does not contain blood clotting protein, in turn not coagulating the blood in case the patient bleeds. This is the... Read More

Understanding Hemophilia Genetics and Implications

Hemophilia is one of the first genetic disorders that have been discussed by ancient scholars. The affected gene can be due to inheritance or the result of a new mutation. In maximum cases however it is due to inheritance. Hemophilia is an X-linked recessive trait. Hemophilia genetics means that for the disorder to surface in a child, both the X chromosomes of a girl child has to carry the trait. On the other hand for a boy child to have the hemophilia genetics, he must inherit the defective X chromosome from either parent, since men have only one X chromosome. Humans have 23 pairs of... Read More

About Hemophilia Inheritance

Hemophilia inheritance is one of the most important causes of hemophilia and that has been discussed below. Humans have 23 pairs of chromosomes. Out of which, one pair of chromosome is responsible for determining the sex of an individual, these are called sex chromosomes. While men have a combination of XY chromosomes, females are XX. Patients suffering from hemophilia have a faulty X- chromosome this can be inherited from either parents or can be the caused due a new mutation. Since women have two X-chromosomes, chances of them being haemophilic are greatly reduced since there is always an... Read More

What Causes Hemophilia Mutation?

Hemophilia can be inherited from the mother and this rare blood disorder is mostly dominant in males especially if the mother is the carrier. If the father has hemophilia and the other is not a carrier, then the son will not likely acquire the same disorder. This disorder can lead to defective genes that can cause impaired blood clotting. The factors 8 and 9 have something to do with this blood disorder. Genes are from the X chromosomes that will determine the gender of a baby. This is hemophilia mutation because F8 and F9 genes can definitely cause hemophilia. Mutation in F8 gene is a... Read More