What is the difference between blood loss, pernicious and sickle anemia and describe their pathophysiology with references.
Anemia is the condition in which the blood lacking enough amount of red blod cells, and this will lead to low hemoglobin and it will lead to decreased delivery of oxygen to cells.
During blood loss the blood circulating through systemic circulation, thus the red blood cell count in blood also reduces due to the excess loss of red blood cells from body and no more red blood cells are produced from the body. This will reduce the number of red blood cells in the body.
Pernicious anemia is a medical condition due to the deficency of vitamin B12 in the body. Vitamin B12 is a essential component for the development of red blood cells, so its deficency lead to decreased production red blood cells and this leads to anemia.
sickle cell anemia, an inherited group of disorders, due to the morphological changes n the red blood cells. Normally the red blood cells are biconcave shape and during sickle cell disease the RBC is in sickle chape. This shape of RBC affect the mobility of cells through capillaries, the sicle shape of cells prevent the free movement through small capillaries. Then the surface area of RBC reduced due to change in shape, so its oxygen carring capacity also reduce. And normal RBCs lifespan is about 90 to 120 days, the sickle cell RBC live for 60 to 80 days only. So the available RBC cells in body are low and is lead to anemia
What is the difference between blood loss, pernicious and sickle anemia and describe their pathophysiology with...
comparison of pernicious anemia and sickle cell anemia.
Describe the morphology of erythrocytes, the mechanism, and primary cause of the following anemias: Pernicious anemia, folate deficiency anemia, iron deficiency anemia, thalassemia, and sickle cell anemia.
Sickle Cell Anemia Sickle cell anemia is the result of a type of mutation in the gene that codes for part of the hemoglobin molecule. Recall that hemoglobin carries oxygen in your red blood cells. The mutation causes these red blood cells to become stiff & sickle-shaped when they release their oxygen. The sickled cells tend to get stuck in blood vessels, causing pain and increased risk of stroke, blindness, damage to the heart & lungs, and other conditions. Analyze...
EXTRA CREDIT Describe Sickle Cell Anemia. Include the part of the blood cell damaged also why it is so dangerous. (4 pts) Explain why when climbing Mt Everest climbers first spend 3 to 5 days approximately 4 the way up the mountain. (4pts)
explain, in detail, the relationship between malaria and sickle-cell anemia. Why is having one sickle-cell allele considered a selective advantage? Is this equally beneficial for someone who is homozygous recessive for sickle-cell? Why or why not? Note: use specific vocabulary to describe your answers (genotype, homozygous d, homozygous r, natural selection, heterozygous, etc)
what is the pathophysiology of anemia?
Sickle-cell anemia is caused by a single point mutation in the hemoglobin of human red blood cells. It is a recessive gene. People who have sickle cell anemia are homozygous recessive and suffer terribly from this disorder. Now I have stated in lecture that mutations are neither good nor bad. Rather it depends on how the mutation effects the survival of the species. If the mutation harms the survival of the species it is bad, if it helps the survival...
My Study on Sickle Cell Anemia Research In 500 words, answer the following questions 1.Select your study sample 2. How have you selected your sample? 3. How will you select your sample population and give the rationale behind your decision Please type the solution on the keyboard so that I can copy and paste Q. No 1. Answer : Sickle cell disease : It is defined as it is a chronic heriditory form of Anemia, in which the red blood...
There is debate as to whether the relationship between the alleles for normal blood and sickle cell anemia should be viewed as having a complete dominance relationship or a co-dominance relationship. Explain both view points. (In your answer define the terms complete dominance and co-dominance).
Sickle-cell anemia is caused by a single point mutation in the hemoglobin of human red blood cells. It is a recessive gene. People who have sickle cell anemia are homozygous recessive and suffer terribly from this disorder. Now I have stated in lecture that mutations are neither good nor bad. Rather it depends on how the mutation effects the survival of the species. If the mutation harms the survival of the species it is bad, if it helps the survival...