This hospital based cross-sectional study describes the number of hemoglobinopathies in population southern Odisha during period and distribution each group hemoglobinopathy found according to their age, sex, clinical signs & symptoms, history consanguinity marriage parents, previous blood transfusion, siblings, socioeconomic status family, groups hematological parameters.

conclusions if such a regimen is approved, it would be a breakthrough in the treatment of hcv in subjects with hemoglobinopathy. more prospective, randomized control trial studies are needed to investigate the efficacy and safety profile of such a regimen. case presentation we described a 16- year-old male patient with sickle-thalassemia who was infected with a hcv. treatment was started with s...

1 Research Center of Thalassemia and Hemoglobinopathy, Jundishapur University of Medical Sciences, Ahvaz, IR Iran 2 Hematology and Oncology Research Center, Tabriz University of Medical Sciences, Tabriz, IR Iran 3 Division of Pharmacology, Utrecht Institute for Pharmaceutical Sciences, Utrecht University, Utrecht, Netherlands 4 Young Researchers Club, Science and Research Branch, Islamic Azad U...

background: hemoglobinopathy and thalassemia are prevalent genetic disorders throughout the world. beta thalassemia is one of these disorders with high prevalence in iran, especially in khuzestan province. in this study, the rate of different mutations in β-globin gene for prenatal diagnosis in fetal samples was evaluated. materials and methods: in this experimental pilot study, 316 fetal sampl...

background: the aim of this perspective study was to assess the frequency of hemoglobinopathy mutational genes among voluntary hemoglobinopathy carrier couples-to-be referred to thalassemia center, shafa hospital, affiliated to ahvaz jondidishapur university of medical sciences (ajuoms), during their first trimester of pregnancy for genetic screening and counseling for prenatal diagnosis (pnd)....