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hereditary elliptocytosis sentence in Hindi

"hereditary elliptocytosis" meaning in Hindihereditary elliptocytosis in a sentence
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  • A schematic diagram representing the relationships between cytoskeletal molecules as relevant to hereditary elliptocytosis.
  • Common hereditary elliptocytosis is the most common form of elliptocytosis, and the form most extensively researched.
  • Almost all forms of hereditary elliptocytosis are autosomal dominant, and both sexes are therefore at equal risk of having the condition.
  • Disorders of the proteins in these membranes are associated with many disorders, such as hereditary spherocytosis, hereditary elliptocytosis, hereditary stomatocytosis, and paroxysmal nocturnal hemoglobinuria.
  • The most important exception to this rule of autosomal dominance is for a subtype of hereditary elliptocytosis called hereditary pyropoikilocytosis ( HPP ), which is autosomal recessive.
  • These mutations have a common end result; they destabilise the Figure 2-A schematic diagram representing the relationships between cytoskeletal molecules as relevant to hereditary elliptocytosis.
  • The incidence of hereditary elliptocytosis is hard to determine, as many sufferers of the milder forms of the disorder are asymptomatic and their condition never comes to medical attention.
  • However relation to membrane structural stability has been implicated in the concurrence of aldolase A deficiency and dominant ( mild ) hereditary elliptocytosis, speculatively also relating to ATP depletion.
  • HPP has been associated with a defect of the erythrocyte membrane protein spectrin and with spectrin deficiency . It was characterized in 1975 . It is considered a severe form of hereditary elliptocytosis.
  • Because it can confer resistance to malaria, some subtypes of hereditary elliptocytosis are significantly more prevalent in regions where malaria is Malayan natives its incidence is 1500-2000 per 10, 000.
  • This variant of haploinsufficiency is only seen in two other human diseases : Erythropoietic protoporphyria, caused by mutations in the FECH gene; and hereditary elliptocytosis, caused by mutations in the spectrin gene.
  • Bite cells and / or blistor cells for oxidative hemolysis, Acanthocytes for pyruvate kinase deficiency or McLeod phenotype, Sickle cells for sickle cell anemia, Spherocytes for immune-mediated hemolysis or hereditary spherocytosis, Elliptocytosis for iron deficiency or hereditary elliptocytosis and schistocytes for intravascular hemolysis.
  • Unlike those with the Leach phenotype of common hereditary elliptocytosis ( see above ), there is a clinically significant reduction in both disease severity and prevalence of malaria in those with SAO . Because of this, the 35 % incidence rate of SAO along the north coast of Madang Province in Papua New Guinea, where malaria in endemic, is a good example of natural selection.
  • For instance, the most common genotype responsible for HPP occurs when the affected individual inherits an ?-spectrin mutation from one parent ( i . e . one parent has hereditary elliptocytosis ) and the other parent passes on an as-yet-undefined defect that causes the affected individual's cells to preferentially produce the defective ?-spectrin rather than normal ?-spectrin.
hereditary elliptocytosis sentences in Hindi. What are the example sentences for hereditary elliptocytosis? hereditary elliptocytosis English meaning, translation, pronunciation, synonyms and example sentences are provided by Hindlish.com.