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Abstract
The term “thalassemia” refers to a group of autosomal-recessive blood diseases charaeterized by a decrease in the synthesis of one of two types of polypeptide chains of globin (α or β), that form a molecule of adult hemoglobin(HbA, α2β2). This leads to a decrease in the filling of erythrocytes with hemoglobin and anemia. In Uzbekistan, the birth rate with this disease is 10-15 per year. At present in the Republic of Uzbekistan, 184 patients with thalassemia are registered at the Research Institute of Hematology and Blood Transfuzion at the Dispensary.
Keywords
anemia
hemoglobinopathy
thalassemia
hemosiderosis
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This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
How to Cite
Zaynutdinova D.L, Qudratova M.F, Qo’ziyeva M.G, Muhammadaminova D.R, & Axtamov A.J. (2022). To Evaluation of Effectiveness of Chelatory Therapy in Patients with Talassemia. Texas Journal of Multidisciplinary Studies, 13, 145–151. Retrieved from https://zienjournals.com/index.php/tjm/article/view/2630
References
- Akperova G. Istoriya izucheniya i reshenia problemy b-thalassemia v Azerbaijan. // Kazakhstan: Scientific and practical medical journal. 2013. 4.: #30. 21-28s.
- Betty Sisla. Management of laboratory hematology. /Pod ed. Practical medicine Vorobeva A. I., 2011. 88-96 p.
- Makhmudova S. A. Novye podkhody k diagnostike i lecheniyu beta-thalassemia u detey // Dissertation 1996. 135s
- Rumyantseva A.G., Tokareva Yu.N., Smetaninoy N.S. Hemoglobinopathies and thalassemic syndromes. /Pod ed. Practical medicine, 2015, 448p.
- Suleymanova D.N., Mamatkulova D.F. Risk of peregruzki sign and chelation therapy and thalassemia patients. //Methodicheskoe posobie. 2017. -30s
- Zaynutdinova D.L., Suleymanova D.N. Dynamics of ferritin indicators during chelator therapy in hemosiderosis // New day in medicine. 2018.3 (23). S 128-132
- More