Gholamreza Hatam; Azra Shamseddin; Farhoud Nikouee
Volume 2, Issue 3 , September 2005, , Pages 177-181
Abstract
Background: Toxoplasmosis is a parasitic disease caused by protozoan, Toxoplasma gondii. Infections of human are common and are usually asymptomatic. The infection may be serious if is transmitted to the fetus during pregnancy. Prophylactic measures, early detection of the infection and treatment can ...
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Background: Toxoplasmosis is a parasitic disease caused by protozoan, Toxoplasma gondii. Infections of human are common and are usually asymptomatic. The infection may be serious if is transmitted to the fetus during pregnancy. Prophylactic measures, early detection of the infection and treatment can avoid congenital toxoplasmosis and many long term effects. Objective: Seroepidemiological study in young girls is useful to determine the prevalence of infection and to design prevention policies for them after marriage and during their pregnancy. This study was carried out in the years 2000-2001 in the region of Fasa of Fars province in the South of Iran, as a descriptive, analytic and cross sectional study. Methods: Serum Samples of 947 students were collected from high school girls of Fasa and studied by enzyme linked immunosorbant assay (ELISA). The positive and negative controls were also used. Results: The seroprevalance rate of toxoplasmosis ranged from 1 to 21 Percent in different parts of Fasa and 10% in all groups. Some variables including age, nutritional habits and contact with domestic cats were studied. Conclusion: The seroprevalence of toxoplasmosis in girls of various high schools of Fasa is different and it may be related to the level of hygiene in different parts of Fasa. Water and food contamination with cat stool in regions with high contact with domestic cats can play an important role in infection rates. People of such areas should eat well-cooked meat to reduce infection.
Mohammad Javad Fattahi; Abdul Mohammad Pezeshki; Maryam Emad; Mohammad Hosein Lohrasb; Azra Shamseddin; Abbas Ghaderi; Mehrnoosh Doroudchi
Volume 2, Issue 2 , June 2005, , Pages 97-102
Abstract
Background: Vitiligo is an acquired skin disorder that selectively destroys melanocytes in epidermis with an unknown etiology. Objective: To investigate the exon 1 A49G polymorphism of cytotoxic T lymphocyte antigen-4 (ctla-4) gene in vitiligo patients. Methods: The A49G polymorphism was ...
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Background: Vitiligo is an acquired skin disorder that selectively destroys melanocytes in epidermis with an unknown etiology. Objective: To investigate the exon 1 A49G polymorphism of cytotoxic T lymphocyte antigen-4 (ctla-4) gene in vitiligo patients. Methods: The A49G polymorphism was detected by Polymerase Chain Reaction-Restriction Fragment Length Polymorphism (PCR-RFLP) method in 101 patients and 208 normal healthy age/ethnicity matched individuals. Results: The frequencies of heterozygote genotypes in patients and controls were found to be 42 (41.6%) of 101 and 85 (40.9%) of 208, respectively. The frequencies of homozygote A and G genotypes were 49 (48.5%) and 10 (9.9%) in 101 patients, whereas, these frequencies in 208 control individuals were 103 (49.5%) and 20 (9.6%), respectively. There was no significant difference between the genotype (P = 0.98) and allele (P = 0.86) frequencies of A49G polymorphism in patients and normal healthy individuals. Conclusion: Our results indicate that in contrast to several immune mediated disorders, there is no association between ctla-4 A49G gene polymorphism and vitiligo.
