Thalassemia Case Study Video
Beta Thalassemia; Causes and Types (minor, major and intermedia) Thalassemia Case StudyThalassemia Case Study - phrase magnificent
A case-control study was performed at Dr. Age- and sex-matched controls were enrolled. The subjects had no blood transfusion, had normal liver function, and had no sign of inflammation. The groups were compared in terms of the levels of hemoglobin Hb , serum ferritin SF , transferrin saturation TS , serum hepcidin, and GDF15 as iron homeostasis parameters. The median SF and TS levels were significantly higher than those in controls The median GDF15 level was significantly higher in patients 2, This may be caused by increased iron absorption due to massive erythropoietic activity, characterized by an increase in GDF15 levels, which does not cause hepcidin suppression. The iron homeostasis response seems to be physiologically indicated by a tendency to increase hepcidin levels. Beta-thalassemia is hereditary anemia that results from defects in globin genes that are inherited in an autosomal recessive pattern. Over time, the combination of hypoxia, increased EPO, and IE creates a vicious circle that induces massive erythroblast expansion in the bone marrow.Either your web browser doesn't support Javascript or it is currently turned off. In the latter case, please Thalzssemia on Javascript support in your web browser and reload this page. Read article at publisher's site DOI : Thalassemia Case Study To arrive at the top five similar articles we use a word-weighted algorithm to compare words from the Title and Abstract of each citation.
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Int Surg87 401 Oct Cited by: 9 articles PMID: Asian J Transfus Sci4 201 Jul Origa R. Cited by: 0 articles PMID: Tamary HDgany O. Europe PMC requires Javascript to function effectively. Recent Activity. Recent history Saved searches. Abstract Available from publisher site using DOI. A subscription may be required. Thalassemia Case Study RS 1. Thalassemiaa articles by 'Rianti'.]
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