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Haemophilia (British English), or hemophilia (American English) [6] (from Ancient Greek αἷμα (haîma) 'blood' and φιλία (philía) 'love of'), [7] is a mostly inherited genetic disorder that impairs the body's ability to make blood clots, a process needed to stop bleeding.
Haemophilia B, also spelled hemophilia B, is a blood clotting disorder causing easy bruising and bleeding due to an inherited mutation of the gene for factor IX, and resulting in a deficiency of factor IX. It is less common than factor VIII deficiency (haemophilia A). [3] Haemophilia B was first recognized as a distinct disease entity in 1952. [4]
Animals with stress (isolated, cortisol levels) show a decrease in neurogenesis and antidepressants have been discovered to promote neurogenesis. Rene Hen and his colleagues at Columbia University ran a study on rats in which they blocked neurogenesis by applying radiation to the hippocampal area to test the efficacy of antidepressants.
Due to routine use of the Hib vaccine in the U.S. since 1990, the incidence of invasive Hib disease has decreased to 1.3/100,000 in children. [51] However, Hib remains a major cause of lower respiratory tract infections in infants and children in developing countries where the vaccine is not widely used.
Canine herpesvirus is an infectious disease that is a common cause of death in puppies less than three weeks old. [7] Pseudorabies (Morbus Aujeszky) is an infectious disease that primarily affects swine, but can also cause a fatal disease in dogs with signs similar to rabies. [8]
[2] [3] However, it can include decreased oxygen-binding ability of each hemoglobin molecule due to deformity or lack in numerical development as in some other types of hemoglobin deficiency. [citation needed] Anemia is the most common disorder of the blood. There are several kinds of anemia, produced by a variety of underlying causes.
It was developed by Jensen et al. 2001 [2] [8] and also published with their own trials, which showed 17.1% of individuals suspected of haemoplasmosis did suffer from this species. [2] Jensen also find none of the asymptomatic controls had this species, although some did suffer from M. haemominutum . [ 2 ]
Because the gene for factor IX is located on the X chromosome (Xq27.1-q27.2), loss-of-function mutations thereof are X-linked recessive: males experience the disease phenotype much more frequently than females. At least 534 disease-causing mutations in this gene have been discovered. [15]
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