The mean cell hemoglobin concentration of your patient is reduced. What type of anemia is this?
Homework Answers
The mean cell hemoglobin concentration refers to the amount of hemoglobin present in the red blood cell.A low level of this indicates that there is inadequate RBC and hemoglobin to carry the iron rich protein which has the capability to carry oxygen to different cells.. This will lead to a type of anemia associated with iron called as iron deficiency anemia. This type of anemia is the most common form of anemia found in every females.
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mean cell hemoglobin concentration of your patient is reduced. What
type of anemia is this?
The mean cell hemoglobin concentration of your patient is 12. reduced. What type of anemia is...
The mean cell hemoglobin concentration of your patient is 12. reduced. What type of anemia is this? Microcytic Macrocytic Нуроchromic Нуpotrophic a. b. c. d.
Sickle Cell Anemia Sickle cell anemia is the result of a type of mutation in the...
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...
Why is electrophoresis with hemoglobin component of 86.5% HbS key test for sickle cell anemia? How...
Why is electrophoresis with hemoglobin component of 86.5% HbS key test for sickle cell anemia? How is sickle cell anemia inherited? Why would reticulocyte percentage increase during a sickle cell attack?
Sickle-cell anemia is caused by a single point mutation in the hemoglobin of human red blood...
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...
A mutation in one of the hemoglobin genes causes sickle cell anemia. The sickle cell allele,...
A mutation in one of the hemoglobin genes causes sickle cell anemia. The sickle cell allele, S, severely reduces fitness in people who are homozygotes, SS. In contrast, people with at least one normal hemoglobin allele, A, do not suffer the effects of sickle cell anemia, even if the individual is a heterozygote, AS. Interestingly, though, in areas with a high rate of malaria, heterozygotes that carry the sickle cell allele have a higher fitness than do individuals that are...
what are the psychosocial stressors/issues coping, strategies, environmental issues for a patient with anemia psychosocial stressors...
what are the psychosocial stressors/issues coping, strategies, environmental issues for a patient with anemia psychosocial stressors of anemia psychosocial stressors of low hemoglobin
Which of the following statements about sickle cell anemia is INCORRECT? Select one: a. Prenatal diagnosis...
Which of the following statements about sickle cell anemia is INCORRECT? Select one: a. Prenatal diagnosis of sickle cell anemia can be made by examination of DNA from fetal cells obtained by amniocentesis. b. Red cells have a shorter than normal survival in the circulation c. No treatment is available. d. Newborn infants homozygous for the sickle cell gene have few symptoms because their red cells also contain a large amount of fetal hemoglobin as well as sickle cell hemoglobin...
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 disorde
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...
A mutation in one of the hemoglobin genes causes sickle cell anemia. The sickle cell allele,...
A mutation in one of the hemoglobin genes causes sickle cell anemia. The sickle cell allele, S, severely reduces fitness in people who are homozygotes, SS. In contrast, people with at least one normal hemoglobin allele, A, do not suffer the effects of sickle cell anemia, even if the individual is a heterozygote, AS. Interestingly, in areas with high rates of malaria, a single Sallele confers some resistance to malarial infection. Suppose there is a population with the observed and...
Sickle-cell Anemia Study Sickle-cell anemia or Sickle-cell disease, is a hereditary disorder. characterized by aryabnormality in...
Sickle-cell Anemia Study Sickle-cell anemia or Sickle-cell disease, is a hereditary disorder. characterized by aryabnormality in the oxygen-carrying hemoglobin molecule in erythrocytes. Sickle-cell conditions have an autosomal recessive pattern of inheritance from parents. The sickle cell defect is a mutation of a single nucleotide of the hemoglobin B gene, which results in glutamic acid being substituted by a different amino acid at position 6. Hemoglobin with this mutation is referred to as Hbs, as opposed to the normal hemoglobin HbA....
The mean cell hemoglobin concentration of your patient is 12. reduced. What type of anemia is this? Microcytic Macrocytic Нуроchromic Нуpotrophic a. b. c. d.
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...
A mutation in one of the hemoglobin genes causes sickle cell anemia. The sickle cell allele, S, severely reduces fitness in people who are homozygotes, SS. In contrast, people with at least one normal hemoglobin allele, A, do not suffer the effects of sickle cell anemia, even if the individual is a heterozygote, AS. Interestingly, though, in areas with a high rate of malaria, heterozygotes that carry the sickle cell allele have a higher fitness than do individuals that are...
Which of the following statements about sickle cell anemia is INCORRECT? Select one: a. Prenatal diagnosis of sickle cell anemia can be made by examination of DNA from fetal cells obtained by amniocentesis. b. Red cells have a shorter than normal survival in the circulation c. No treatment is available. d. Newborn infants homozygous for the sickle cell gene have few symptoms because their red cells also contain a large amount of fetal hemoglobin as well as sickle cell hemoglobin...
A mutation in one of the hemoglobin genes causes sickle cell anemia. The sickle cell allele, S, severely reduces fitness in people who are homozygotes, SS. In contrast, people with at least one normal hemoglobin allele, A, do not suffer the effects of sickle cell anemia, even if the individual is a heterozygote, AS. Interestingly, in areas with high rates of malaria, a single Sallele confers some resistance to malarial infection. Suppose there is a population with the observed and...
Sickle-cell Anemia Study Sickle-cell anemia or Sickle-cell disease, is a hereditary disorder. characterized by aryabnormality in the oxygen-carrying hemoglobin molecule in erythrocytes. Sickle-cell conditions have an autosomal recessive pattern of inheritance from parents. The sickle cell defect is a mutation of a single nucleotide of the hemoglobin B gene, which results in glutamic acid being substituted by a different amino acid at position 6. Hemoglobin with this mutation is referred to as Hbs, as opposed to the normal hemoglobin HbA....
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