"Hemophilia" Essays and Research Papers

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    Multiple-Choice Questions 1. Chromosomes other than those involved in sex determination are known as a. nucleosomes b. heterosomes c. alleles d. autosomes e. liposomes Section: 11.1 Bloom’s: knowledge Ans: d 2. Sex chromosomes a. determine sex b. vary from one sex to another c. carry some genes that have nothing to do with sex d. were unknown to Mendel e. all of these Section: 11.1 Bloom’s: knowledge Ans: e 3. Which of the following designates a normal human female?

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    THE ROMANOV FAMILY 1) Hemophilia is a kind of sex-linked disorder. The Romanovs actually have a child with symptoms of hemophilia. It is possible‚ that a family with the same genotypes have no children with hemophilia‚ because in Alexandra’s family this disorder was present then the chance of having a normal child was 50%. This is true each time a child is born to the family. 2) Skeletons can be identified trough few techniques in order to determine the age‚ sex‚ and race of the decedent.

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    The royal line of England during Queen Victoria’s reign was afflicted with hemophilia‚ mainly due to a lack of genetic diversity in the royalty of the era. Hemophilia was a death sentence back then‚ as any scrape‚ bruise‚ or trauma could cause uncontrollable bleeding as the wound did not clot. Females‚ especially‚ were prone to death at the onset of menses‚ as their own

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    Anatomy: Blood Clotting

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    Cited: "All About Hemophilia / Haemophilia." Medical News Today. MediLexicon International‚ 30 Dec. 0031. Web. 09 Aug. 2012. <http://www.medicalnewstoday.com/info/hemophilia/what-is-coagulation.php>. "American Society of Hematology." Blood Clots. N.p.‚ n.d. Web. 07 Aug. 2012. <http://hematology.org/Patients/Blood-Disorders/Blood-Clots/5233

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    that create water deficit. Other commons causes are: 9. DDVAP is a synthetic analogue of the natural pituitary hormone 8-arginine vasopressin (ADH)‚ an antidiuretic hormone affecting renal water conservation. It is indicated for patients with hemophilia A with factor

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    Medical Benefits and Consequences in Genetic Engineering Today scientists are experimenting with gene therapy as a way to permanently help people who have hemophilia and other inherited diseases. Gene therapy involves inserting healthy genes into human cells to correct or prevent diseases. When genes are introduced into body cells other than eggs and sperm‚ this is called somatic cell gene therapy. Any effects are limited to the person receiving the therapy as the new genes are not passed on

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    saving people’s lives who suffer from life threatening injuries or illnesses. Doctors and patients are exploring alternative treatments that use either no blood or small fractions of the patient’s own blood. The first research on hemophilia started in 1803. Hemophilia is a condition where blood is not able to clot‚ causing the injured to bleed severely. There has been a ton of different ways to try and stop bleeding throughout the years. Diluting snake venom was used to clot blood in the 1930’s

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    Biology Mrs. Linda December 19‚ 1994 There are thousands of cases of sex linked and sex influenced diseases worldwide. These diseases can range from a social inconvenience‚ to a fatal ailment. In sex linked diseases‚ like Muscular Dystrophy‚ hemophilia and color blindness‚ only males are affected. When a man infected with a sex linked disease has children‚ all his sons are normal‚ but all of his daughters are carriers. When a carrier woman and an uninfected man have children‚ half of the sons

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    HEMOSTASIS Hemostasis: drives from the Greek meaning “The stoppage of blood flow”. a process which causes bleeding to stop‚ meaning to keep blood within a damaged blood vessel. It is the first stage of wound healing. Hemostasis can be divided into two stages: Primary and Secondary. 1- Primary hemostasis includes the platelet and vascular response to vessel injury. 2- Secondary hemostasis includes the coagulation factors response to such injury. Together‚ platelets‚ vessels‚ and coagulation

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    large family from the Aland Islands had enlarged bruising and extended incidents of bleeding. The seriousness of the bleeding varied between family members and ranged from mild to severe. What differentiated this bleeding disorder from classical hemophilia was that it did not appear to be linked with muscle and joint bleeding‚ and it affected both women and men. Dr. von Willebrand named this disorder hereditary pseudohemophilia (Andres 1554). Pseudohemophilia‚ commonly known as von Willebrand disease

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