نتایج جستجو برای: thalasemia
تعداد نتایج: 66 فیلتر نتایج به سال:
Present study was aimed to explore the effect of (TA)n UGT1A1 gene promoter polymorphism on bilirubin metabolism, bilirubinaemia, predisposition to cholelithiasis and subsequent cholecystectomy, in Sickle-Cell Anemia (SCA) and beta-Thalasemia major (bTH) in Kuwaiti subjects compared to other population. This polymorphism was analyzed and correlated to total bilirubin and cholelithiasis in 270 a...
Introduction: The β-thalassaemias represent a heterogenous group of diseases resulting from decreased β-globin mRNA expression and imbalanced alpha/betaglobin chain synthesis which are clinically manifested by ineffective erythropoiesis and excessive hemolysis. Increasing levels of hemoglobin F (HbF) by improving the balance in globin chain synthesis. Hydroxyurea (HU), as an effective with lo...
Abstrak: Perbandingan Hasil Pemeriksaan Hematologi Jumlah Hemoglobin Pada Sampel Darah Pasien Talasemia Dengan Antikoagulan K2edta Segera Dan Setelah Ditunda 4 Jam Post Sampling Di RSUD Dr. H. Abdul Moeloek Bandar Lampung. Talassemia adalah penyakit kelainan pada rantai hemoglobin. Salah satu pemeriksaan thalassemia darah lengkap untuk mengetahui kadar Hb dalam penentuan kebutuhan transfusi dar...
Background and purpouse : Thalasemia major is one the most prevalent congenital anemia. These patients recieved much rate of iron, due to frequent blood transfusion. Indocrine disorders are prevalent due to replacement of iron in indocrinal gland system, example can be of hypogonadism. In this study the delay of puberty in thalasemic patients of Gorgan city and its relevance to the rate of fe...
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