Another Name for Hemophilia is the "Royal Disease" because of Queen Victoria's male descendants. Many of the male sons or grandsons of Victoria's family died from blood loss.
Yes hemophilia is a inheerited bleeding dissorder. i read it from my medical book. hemophilia means blood love and can be passed down from mother to daughter. or in some cases mother to son. it is more common for it to passed to daughters. I hope this helped. :)
Grand Duchess ANASTASIA and her sisters were probably carriers of the hemophilia gene but did not suffer from the effects of hemophilia. Males suffer from hemophilia. In rare cases girls do suffer but that is only when both parents carry the mutated gene
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.
A male with hemophilia does in fact carry the genes and can pass them on to his daughters, so yes, some boys (if they have hemophilia) are carriers.
Hemophilia is treated by replacing the missing clotting factors intravenously.
Hemophilia ia a sex linked disorder that is normally recessive. There are many cases however where trait shows "incomplete or shared" dominance. In these cases the females will have lowered percentages of the clotting factor proteins and may for all intents and purposes be considered mild or moderate hemophiliacs themselves.
No, the most commonly talked about form of hemophilia is a genetic disorder that simply prevents the person't liver from producing very specific proteins called clotting factors. There is also blood disorders referred to as acquired hemophilia. The cases of acquired hemophilia is on the rise due to the vast number of blood thinning and liver damaging medications on the market today. Things such as extensive liver damage and certain medications can also inhibit clotting factor production or effectiveness. In neither of these cases is hemophilia caused by a pathogen though.
Hemophilia A affects between one in 5,000 to one in 10,000 males in most populations. Hemophilia B occurs in one in 40,000 to 50,000. The prevalence of hemophilia is estimated to be 13.4 cases per 100,000 U.S. males (10.5 hemophilia A and 2.9 hemophilia B). By race/ethnicity, the prevalence is 13.2 cases in 100,000 among white males, 11.0 among African-American males, and 11.5 among Hispanic males. Hemophilia C occurs primarily among individuals of Jewish descent.For the source and more detailed information concerning this request, click on the related links section (Answers.com) indicated below this answer box.Hemophilia A affects between one in 5,000 to one in 10,000 males in most populations. Hemophilia B occurs in one in 40,000 to 50,000. The prevalence of hemophilia is estimated to be 13.4 cases per 100,000 U.S. males (10.5 hemophilia A and 2.9 hemophilia B). By race/ethnicity, the prevalence is 13.2 cases in 100,000 among white males, 11.0 among African-American males, and 11.5 among Hispanic males. Hemophilia C occurs primarily among individuals of Jewish descent.For the source and more detailed information concerning this request, click on the related links section (Answers.com) indicated below this answer box.Hemophilia A affects between one in 5,000 to one in 10,000 males in most populations. Hemophilia B occurs in one in 40,000 to 50,000. The prevalence of hemophilia is estimated to be 13.4 cases per 100,000 U.S. males (10.5 hemophilia A and 2.9 hemophilia B). By race/ethnicity, the prevalence is 13.2 cases in 100,000 among white males, 11.0 among African-American males, and 11.5 among Hispanic males. Hemophilia C occurs primarily among individuals of Jewish descent.For the source and more detailed information concerning this request, click on the related links section (Answers.com) indicated below this answer box.Hemophilia A affects between one in 5,000 to one in 10,000 males in most populations. Hemophilia B occurs in one in 40,000 to 50,000. The prevalence of hemophilia is estimated to be 13.4 cases per 100,000 U.S. males (10.5 hemophilia A and 2.9 hemophilia B). By race/ethnicity, the prevalence is 13.2 cases in 100,000 among white males, 11.0 among African-American males, and 11.5 among Hispanic males. Hemophilia C occurs primarily among individuals of Jewish descent.For the source and more detailed information concerning this request, click on the related links section (Answers.com) indicated below this answer box.Hemophilia A affects between one in 5,000 to one in 10,000 males in most populations. Hemophilia B occurs in one in 40,000 to 50,000. The prevalence of hemophilia is estimated to be 13.4 cases per 100,000 U.S. males (10.5 hemophilia A and 2.9 hemophilia B). By race/ethnicity, the prevalence is 13.2 cases in 100,000 among white males, 11.0 among African-American males, and 11.5 among Hispanic males. Hemophilia C occurs primarily among individuals of Jewish descent.For the source and more detailed information concerning this request, click on the related links section (Answers.com) indicated below this answer box.Hemophilia A affects between one in 5,000 to one in 10,000 males in most populations. Hemophilia B occurs in one in 40,000 to 50,000. The prevalence of hemophilia is estimated to be 13.4 cases per 100,000 U.S. males (10.5 hemophilia A and 2.9 hemophilia B). By race/ethnicity, the prevalence is 13.2 cases in 100,000 among white males, 11.0 among African-American males, and 11.5 among Hispanic males. Hemophilia C occurs primarily among individuals of Jewish descent.For the source and more detailed information concerning this request, click on the related links section (Answers.com) indicated below this answer box.
Some famous cases of false imprisonment include Lois Austin and Geoffrey Saxby in Oxford Circus, London, and Enright v Groves, in which a woman was arrested without a legitimate cause.
replace the clotting factor in the veins
Hemophilia has several common symptoms and these include bleeding of the joints and muscles, and prolonged bleeding. Bleeding is not typically faster or different to someone without hemophilia but it takes much longer to stop, typically, and this is the main symptom of the illness.
Hemophilia is not acquired from microorganisms. Hemophilia is typically a genetic disorder that can either be inherited or result from a random mutation. In rare cases non genetic forms (that can not be inherited or passed on) of hemophilia can be acquired due to liver impairment, and certain medications.