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.
no it dose not
No. Marfan syndrome is found equally across all ethnicities and genders.
No, it affects all ethnic groups.
Yes, it is possible to develop hemophilia later in life, although it is rare. Acquired hemophilia can occur in adults due to certain medical conditions or medications that interfere with the body's ability to clot blood.
Hemophilia does not occur more frequently in any specific blood type. It is a genetic disorder primarily linked to mutations in the genes responsible for producing clotting factors, particularly factor VIII (hemophilia A) and factor IX (hemophilia B). The condition is inherited in an X-linked recessive manner, meaning it predominantly affects males regardless of their blood type. Therefore, blood type does not influence the incidence of hemophilia.
hemophilia
Hemophilia is a X linked recessive disorder. Usually the mother is an unaffected carrier and her son unfortunately receives the X chromosome in which hemophilia is linked to.
recessive sex-linked, X chromosome disorders, haemophilia is more likely to occur in males than females.
Angelman syndrome can affect people of any ethnic background. It is caused by a genetic mutation on chromosome 15 and can occur in individuals regardless of their ethnic origins.
Genetic hemophilia is a life-long chronic condition. A person would have it all of their life, from birth to death. Acquired hemophilia happens as a result of some other circumstance and is not directly linked to age. A person may get acquired hemophilia from causes such as extensive liver damage or certain medications. Since these conditions normally occur in older populations it generally trends that way but is no way limited to that age set.
Because the gene that causes hemophilia is located on the X chromosome, so it will occur in males more frequently than in females.
Ethnogenesis refers to the process by which a distinct ethnic group comes into existence. This can occur through a variety of factors such as migration, intermarriage, and cultural diffusion, which contribute to the formation of a new sense of shared identity among a group of people. Ethnogenesis can be a complex and dynamic process that evolves over time.