Q: Disseminated intravascular coagulation (DIC) is associated with which of the following conditions?
A: Disseminated intravascular coagulation (DIC) is a rare condition characterized by abnormal blood…
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Q: thalassemia is occur due to .40 * hemoglobinopathies TO
A: Anemia It is hematological condition characterized by qualitative or quantitative decrease in number…
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A: Matched answers: COLUMN - A…
Q: Discuss the effects of several virulence factors that act on white blood cells.
A: Introduction: Virulence is the degree of pathogenicity caused by a microbe and the ability to cause…
Q: What causes hemolytic disease of the newborn (erythroblastosis fetalis)? Why does the condition not…
A: Rhesus factor (Rh) is an antigen present on the red blood cells of humans and some other primates.…
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A: Sickle cell anaemia is genetic disorder resulting due to mutation in hemoglobin molecules (globin…
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Q: NURSING QUESTION... List all the possible risk factors for non communicable diseases. Thanks.
A: Non communicable disease can't communicate /transfer from one to another person.
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Q: State the probability that a child with a carrier mother willhave hemophilia A.
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A:
Q: explain pleiotropy in sickle cell disease.
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Q: What characteristics cytochemical is positive in Hairy Cell Leukemia?
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A: The undesirable reactions are produced because the overreaction of the immune system is defined by…
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A: Sickle cell anaemia is a type of disease that is caused due to abnormal hemoglobin known as sickle…
Q: Define hematocrit, and explain how the medical definition differs from the clinical usage.
A: Blood is a bodily fluid in humans and other species that transfers metabolic waste products away…
Q: why are the children of Rh positive mothers not at risk for this disease erythroblastosis fetalis?
A: When a woman is pregnant, it’s possible that her baby’s blood type is not very compatible with her…
Q: Is sickle cell rare or prevalent in the human population
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Q: Describe the roles of carbohydrates as antigens in the human body and in RBC
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Q: Give three or more examples of diseases where there is: a) decreased hematocrit; 1 2 3 b)…
A: A hematocrit test is a test which come under CBC (complete blood count) measuring the red blood…
Q: why are the children of Rh positive mothers not at risk for this erythroblastosis fetalis
A: Hemolytic disease of the newborn also called Erythroblastosis fetalis. This is considered as the…
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A: Introduction- Hematology is a branch of medicine which deals with the study of blood and components…
Q: Why do children with thalassemia major develop cardiovascular complications?
A: Blood is a liquid connective tissue with formed elements.
Q: Punnett Squares to Show the different ways a person can inherit/pass on the disorder (Sickle Cell…
A: Sickle Cell Anemia: A series of diseases which leads to red blood cells to disintegrate and become…
Q: What Rh antigen is present in the red blood cells of this type of blood?
A: Answer- Rh antigens is the rhesus factor Protein) that is present on the surface of RBC in those…
Q: Could a person with type B+ blood safely receive a blood transfusion of O- blood? Yes No
A: Blood is a liquid substance which flows in the blood vessels and carry nutrients and oxygen to the…
Q: What is the rationale for a blood transfusion in a pediatric patient with Sickle Cell Disease
A: Sickle cell anaemia is a autosomal recessive type of disease that is caused by the genetic mutation…
List 3 differences between sickle cell and b-thalassemia
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- Give three or more examples of diseases where there is: a) decreased hematocrit; 1 2 3 b) increased hematocrit. 1 2 3 and explain why those diseases in under that categoryDefine what is meant by the following statement: Multiple myeloma is heterogeneous.What is sickle cell disease? Describe its effects at a protein, cellular and organismal level.
- A 2-year-old black girl is being seen by the hematologist after her pediatrician found her to be severely anemic with splenomegaly and jaundice. Her mother gives a possible history of a “blood problem” in her family but doesn’t know for sure. Her hemoglobin electrophoresis was normal, and the complete blood count (CBC) revealed a normocytic anemia. The platelet and white blood cell counts are normal. On the peripheral smear, there are many bizarre erythrocytes, including spiculated cells. A diagnosis of pyruvate kinase deficiency is made. In the RBCs of the patient described above, which of the following would be expected? And give the explanation. (3 sentences) ADP to ATP ratios would be elevated above normal. NADP+ would increase relative to NADPH. Ribulose 5-phosphate levels would decrease. NADH to NAD+ ratios would decrease. Methemoglobin levels would increase.Discuss the effects of several virulence factors that act on white blood cells.Why is DNA testing used for a patient with sickle cell anemia?
- d) Folate and vitamin B12 deficiencies cause megaloblastic changes in the bone marrow of a patient with a macrocytic anaemia. State four causes of folate deficiency.In humans, as well as with many other animals, sex is determined by special sex chromosomes. An individual containing two X chromosomes is a female, while an individual possessing an X and Y chromosome is a male. he sex chromosomes bear alleles for traits. Sex linkage applies to genes that are located on the sex chromosomes. These genes are considered sex-linked because their expression and inheritance patterns differ between males and females. The genes present on the X chromosome are said to be X linked. Many more genes are present on the X chromosome than found on the Y chromosome. Nonetheless, those genes found on the Y chromosome are said to be Y linked. The Y chromosome is smaller than its homologue, the X chromosome. Consequently, most of the loci present on the X chromosome are absent on the Y chromosome. 1. In humans, hemophilia is a sex linked trait. Females can be normal, carriers, or have the disease. Males will have the disease or not (but they won't be ever carriers) XH…BACKGROUND A 2-year-old black girl is being seen by the hematologist after her pediatrician found her to be severely anemic with splenomegaly and jaundice. Her mother gives a possible history of a “blood problem” in her family but doesn’t know for sure. Her hemoglobin electrophoresis was normal, and the complete blood count (CBC) revealed a normocytic anemia. The platelet and white blood cell counts are normal. On the peripheral smear, there are many bizarre erythrocytes, including spiculated cells. A diagnosis of pyruvate kinase deficiency is made. Pyruvate kinase deficiency (PKD) can be inherited in an autosomal recessive manner, which means that a child must inherit a gene with the disease-causing mutation from both parents in order for the disorder to be inherited. The PLKR gene regulates the synthesis of the pyruvate kinase enzyme, which is located in the liver and red blood cells. Pyruvate kinase deficiency (PKD) is a rare genetic disorder characterized by the premature…