All the affected individuals are sons, strongly suggesting that the defect Hemophilia essay a sex linkage trait. People with hemophilia are born with the disorder and have it all of their lives.
In addition, all daughters of men with hemophilia are carriers, but his sons are unaffected. Hemophilia occurs almost exclusively in men. These treatment centers are staffed with many hematologists, doctors, and nurses to help care for people with this bleeding disorder.
To determine a sex linkage inheritance of a defective trait, look at a family pedigree to notice the similarities and patterns of the trait throughout the family pedigree for example the pedigree below: The Jewish physician Moses Maimonides applied this ruling to the sons of a woman who had married twice, thus apparently appreciating the hereditary nature of the condition.
These are only some of the kinds of bleeding involved in hemophilia. Hemophilia is the most common hereditary blood disorder. Bleeding inside other parts of the body, such as the brain, throat, and abdomen can be life-threatening. Because the genetic defect occurs on the X chromosome, women are carriers of hemophilia but rarely have the disorder.
Severe hemophilia is actually the most common form.
When these cells plug up a cut, they release chemicals that attract more platelets to the site to stop the bleeding. Clotting factors can be given as needed or when an affected person is bleeding.
There are about 20, hemophilia patients in the United States. This leads to excessive bleeding even for the smallest cut. There are two types of hemophilia, A and B Christmas Disease.
There also is a fifty percent chance that the daughters of a female carrier will be carriers of hemophilia. This is why the symptom of hemophilia is severe bruising.
Hemophilia is a very rare disorder. There are several different inherited forms of hemophilia are known, each deficient on one of the steps in the steps in the pathway that forms fibrinogen, the blood clot protein.
Essay UK - http: For mild cases — protect joints 3. Kids Health A common treatment for hemophilia is to go to a comprehensive hemophilia treatment center HTC.Hemophilia is an inherited medical condition where the blood does not clot properly.
Hemophiliacs Hemophilia essay people with hemophilia, lack a protein called a clotting factor that works with platelets to stop bleeding at the site of an injury. Hemophilia Essay - Hemophilia is a rare genetic blood clotting disorder that primarily affects males.
People living with hemophilia do not have enough of, or are missing, one of the blood clotting proteins naturally found in blood. - Hemophilia Manitoba Hemophilia Manitoba, or hemophilia, is a sex-linked genetic disorder that is effecting about 20, Americans, most of which males. A person with hemophilia either has an inactive or inadequate supply of one of several blood factors needed for blood to clot.
Hemophilia is the oldest known hereditary bleeding disorder. There are two types of hemophilia, A and B (Christmas Disease). Low levels or complete absence of a blood protein essential for clotting causes both. Patients with hemophilia A lack the blood clotting protein, factor VIII, and those with hemophilia B /5(1).
Mar 04, · Sexualy Transmited Diseases: Hemophilia Essay Words | 7 Pages Hemophilia is a genetic bleeding disorder that slows down the clotting process of one’s blood.
Hemophilia Essay - Hemophilia is a sex-linked hereditary bleeding disorder in which it takes a long time for the blood to clot and abnormal bleeding occurs. It is a hereditary blood coagulation disorder caused by a deficient activity of plasma protein factor thirteen and nine, which affects the clotting property of blood.Download