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Jalil Kardan , Hossein Kazemian, Mohammad Mehdi Feizabadi,
Volume 17, Issue 2 (5-2014)
Abstract

Nontuberculous mycobacteria (NTM), also known as atypical mycobacteria or mycobacteria other than tuberculosis are environmental organisms that are normally found in soil and water. Many of the mycobacterial species that have been described in the past decade are involved in human diseases, especially in patients with AIDS and immunocompromised HIV-negative patients. In this study, pathogenicity and clinical significance of new species of mycobacteria were evaluated. A total of 63 new species of non-tuberculosis mycobacteria, recognized in the past ten years (2003-2013), were classified in different Runyon groups. Approximately, 40 isolates were reported to infect human. Of these, 27 (67.5%) were non-chromogenic and 13 (32.5%) were scotochromogenic. The majority of the 40 isolates belong to the slow grower group. Photochromogenic species were not pathogenic to human. The most frequent infections included respiratory infections in elderly people and cervical lymphadenitis in children caused by Mycobacterium kyorinense and Mycobacterium mantenii, respectively. NTM also causes disseminated infections, the most frequent agents of which are M. boenickei, M. houstonense, M. neworleansense, and M. brisbanense in immunocompromised HIV-negative persons. Some of the NTMs, such as Mycobacterium riyadhense, are considered the primary pathogens for human. Considering the progressive spread of HIV co-infected mycobacteria in recent years, accurate identification of these agents’ pathogenicity, drug resistance, and appropriate treatment in epidemic regions, such as Iran, is essential.


Ali Yar Piruzi, Mohammad Jafari, Mirzakhalil Bahmani, Mohammad Azadi, Mohammad Mehdi Feizabadi, Rouhi Afkari,
Volume 18, Issue 1 (4-2015)
Abstract

Background: Glucose-6- phosphate Dehydrogenase enzyme (G6PD) is an enzyme deficiency that is transported inheritably. The lack of this enzyme decreases the energy revival of red blood cells and leads to Hemolysis which is the cause of severe neonatal jaundice. This study aims to investigating glucose-6-phosphate dehydrogenase deficiency, hyperbilirubinemia, and blood incompatibility in newborn babies in larestan city, located in south of Fars province, following the newborn screening national plan.

Materials and Methods: This study is a cross-sectional and descriptive study on 12079 newborns in larestan city that referred to the screeing center from the start of 2010 to the end of 2012. The blood samples were taken from the newborns' heels and were evaluated through G6PD tluorescent spot test. They were examined regarding their blood group, hematocrit, hemoglobin, Coombs test, reticulocyte count and bilirubin levels as well as demographic information.

Results: In this research, among the 12079 screened newborns, 2345 ones showed G6PD deficiency with a prevalence of 19.41 which is a high percentage in comparison to those of other cities in Iran. The prevalence of O+ blood group among sick babies and their mothers was significantly higher than of other blood groups. (60% and 56%, respectively). The Hyperbilirubinemia and the indirect coombs tests were positive in 52% and 12% of the sick babies, respectively.

Conclusion: The prevalence percentage of lack of this enzyme in girls of Larestan city is a little higher than in boys, even though since this disease depends on X, it should be more prevalent in boys.



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