Understansing haemophilia essay

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Understansing haemophilia essay

In the human body, each cell contains 23 pairs of chromosomes, one of each pair inherited through the egg from the mother, and the other inherited through the sperm of the father.

Of these chromosomes, those that determine sex are X and Y.

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Females have XX and males have XY. In addition to the information on sex, 'the X chromosomes carry determinants for a number of other features of the body including the levels of factor VIII and factor IX. When this happens, the protein factors needed for normal blood Understansing haemophilia essay are effected.

In males, the single X chromosome that is effected cannot compensate for the lack, and hence will show the defect. In females, however, only one of the two chromosomes will be abnormal. There are two types of haemophilia, haemophilia A and B.

In most of the cases, this coagulant protein is reduced but in a rare amount of cases, this protein is present by immunoassay but defective. Haemophilia A is the most common severe bleeding disorder and approximately 1 in 10, males is effected. The most common types of bleeding are into the joints and muscles.

Haemophilia is severe if the factor VIII: Those with mild haemophilia bleed only in response to major trauma or surgery. As for the patients with severe haemophilia, they can bleed in response to relatively mild trauma and will bleed spontaneously.

In haemophiliacs, the levels of the factor VIII: If the plasma from a haemophiliac person mixes with that of a normal person, the Partial thromboplastin time PTT should become normal.

The standard treatment of the haemophiliacs is primarily the infusion of factor VIII concentrates, now heat-treated to reduce the chances of transmission of AIDS.

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When major surgery is to be performed, one raises the factor VIII: This sex-linked disease is caused by the reduced amount of the factor IX.

Unlike haemophilia A, the percentage of it's occupance due to an abnormally functioning molecule is larger. Unlike factor VIII concentrates which have a half-life of 12 hours, the half-life of factor IX concentrates is 18 hours.

In addition, factor IX concentrates contain a number of other proteins, including activated coagulating factors that contribute to a risk of thrombosis.

Therefore, more care is needed in haemophilia B to decide on how much concentration should be used.Hemophilia a Bloody Disease Hemophilia is a bleeding disorder caused by a hereditary X-linked recessive gene disorder that causes blood to be thin due to the inability to clot normally.

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There are two types of Hemophilia. Essay on importance of education in our life ivan van sertima they came before columbus essay essay writing com anies caprioska descriptive essay modernism essays and criticism crossword an anthropologist on mars essay summary understanding essay umi dissertations available essay about life on other planets proof the tell tale heart symbolism.

Haemophilia, or hemophilia is a group of inherited blood disorders in which the blood does not clot properly. Known as a rare disease to individuals, Haemophilia has two main inheritable types, Haemophilia and Haemophilia B.

Understansing haemophilia essay

Haemophilia is due in part to defective blood vessels, coagulation mechanisms or blood platelets. Understansing Haemophilia Essay - Introduction to Haemophilia Haemophilia is a term that is used to describe a collection of hereditary blood disorders which has a lifetime defect in the clotting method of the blood.

Haemophilia Essays

It is estimated that 1 in men have haemophilia. Essay about Understanding Haemophilia - Understanding Haemophilia In the human body, each cell contains 23 pairs of chromosomes, one of each pair inherited through the egg from the mother, and the other inherited through the sperm of the father.

Read this Science Essay and over 88, other research documents. Hemophilia.

Understansing haemophilia essay

Hemophilia is the oldest known hereditary bleeding disorder. There are two types of hemophilia, A and B (Christmas Disease).


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