elliptocytosis वाक्य
उदाहरण वाक्य
मोबाइल
- Some of these disorders are known by fanciful and cryptic names like sickle-cell anemia, thalassaemia, glucose-6-phosphate dehydrogenase deficiency, ovalocytosis, elliptocytosis and loss of the Gerbich antigen and the Duffy antigen.
- The contiguous gene deletion syndrome is characterised by Alport syndrome ( A ), intellectual disability ( M ), midface hypoplasia ( M ), and elliptocytosis ( E ), as well as generalized hypoplasia and cardiac abnormalities.
- 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.
- 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.
- A genotype at one locus that produces a phenotype that at some levels of resolution is indistinguishable from that produced by another genotype; two types of elliptocytosis that are genocopies of each other, but are distinguished by the fact that one is linked to the Rh blood group locus and the other is not.
- 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.
- Consequences included natural selection for sickle-cell disease, thalassaemias, glucose-6-phosphate dehydrogenase deficiency, Southeast Asian ovalocytosis, elliptocytosis and loss of the Gerbich antigen ( glycophorin C ) and the genetic resistance ( sickle-cell disease, thalassaemias, and glucose-6-phosphate dehydrogenase deficiency ) were present in the Mediterranean world by the time of the Roman Empire, about 2000 years ago.
- The form discussed here is the one found in the 1950s to be linked to Rh blood group and more recently shown to be caused by a defect in protein 4.1 .'Rh-unlinked'forms of elliptocytosis are caused by mutation in the alpha-spectrin gene ( MIM 182860 ), the beta-spectrin gene ( MIM 182870 ), or the band 3 gene ( MIM 109270 ) [ supplied by OMIM ].
- अधिक वाक्य: 1 2
elliptocytosis sentences in Hindi. What are the example sentences for elliptocytosis? elliptocytosis English meaning, translation, pronunciation, synonyms and example sentences are provided by Hindlish.com.