A report on Malaria, Hemolytic anemia and Red blood cell
Hemolytic anemia is a form of anemia due to hemolysis, the abnormal breakdown of red blood cells (RBCs), either in the blood vessels (intravascular hemolysis) or elsewhere in the human body (extravascular).
- Hemolytic anemiaAcquired hemolytic anemia is also encountered in burns and as a result of certain infections (e.g. malaria).
- Hemolytic anemiaThe presentation may include headache, fever, shivering, joint pain, vomiting, hemolytic anemia, jaundice, hemoglobin in the urine, retinal damage, and convulsions.
- MalariaIn the blood, the merozoites rapidly invade individual red blood cells, replicating over 24–72 hours to form 16–32 new merozoites.
- MalariaLipid rafts that have been implicated in cell signaling events in nonerythroid cells have been shown in erythroid cells to mediate β2-adregenic receptor signaling and increase cAMP levels, and thus regulating entry of malarial parasites into normal red cells.
- Red blood cellHemolysis is the general term for excessive breakdown of red blood cells. It can have several causes and can result in hemolytic anemia.
- Red blood cell3 related topics with Alpha
Anemia
1 linksAnemia or anaemia (British English) is a blood disorder in which the blood has a reduced ability to carry oxygen due to a lower than normal number of red blood cells, or a reduction in the amount of hemoglobin.
Causes of increased breakdown include genetic disorders such as sickle cell anemia, infections such as malaria, and certain autoimmune diseases.
There may be signs of specific causes of anemia, e.g. koilonychia (in iron deficiency), jaundice (when anemia results from abnormal break down of red blood cells – in hemolytic anemia), nerve cell damage (vitamin B12 deficiency), bone deformities (found in thalassemia major) or leg ulcers (seen in sickle-cell disease).
Glucose-6-phosphate dehydrogenase deficiency
1 linksMost common enzyme deficiency worldwide, is an inborn error of metabolism that predisposes to red blood cell breakdown.
Most common enzyme deficiency worldwide, is an inborn error of metabolism that predisposes to red blood cell breakdown.
Most people who develop symptoms are male, due to the X-linked pattern of inheritance, but female carriers can be affected due to unfavorable lyonization or skewed X-inactivation, where random inactivation of an X-chromosome in certain cells creates a population of G6PD-deficient red blood cells coexisting with unaffected red blood cells.
People with G6PD deficiency are therefore at risk of hemolytic anemia in states of oxidative stress.
A side effect of this disease is that it confers protection against malaria, in particular the form of malaria caused by Plasmodium falciparum, the most deadly form of malaria.
Spleen
0 linksOrgan found in all vertebrates.
Organ found in all vertebrates.
The spleen plays very important roles in regard to red blood cells (erythrocytes) and the immune system.
It may be caused by sickle cell anemia, sarcoidosis, malaria, bacterial endocarditis, leukemia, polycythemia vera, pernicious anemia, Gaucher's disease, leishmaniasis, Hodgkin's disease, Banti's disease, hereditary spherocytosis, cysts, glandular fever (mononucleosis or 'Mono' caused by the Epstein–Barr virus, infection from cytomegalovirus), and tumours.
Splenomegaly can result from antigenic stimulation (e.g., infection), obstruction of blood flow (e.g., portal vein obstruction), underlying functional abnormality (e.g., hemolytic anemia), or infiltration (e.g., leukemia or storage disease, such as Gaucher's disease).