The incidence of alpha-thalassemia in Setif, Algeria

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چکیده

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منابع مشابه

The incidence of alpha-thalassemia in Setif, Algeria.

Thalassemias are hereditary anemia syndromes occurring due to erroneous producing of globin chain of hemoglobin. Thalassemia syndromes are named according to the type of the affected globin chain. The most common types of thalassemia are alpha thalassemia and beta thalassemia. In α-thalassemia, α-globin chain production is either by decreased or completely disappeared. The gene encoding the α-g...

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The Incidence of Alpha-Thalassemia in Iraqi Turks

The frequency of alpha-thalassemia was 3.6% among Turkish newborns in a study that employed globin gene mapping analysis of DnA [4]. In our study, in 13 out of 205 cord blood samples alpha-thalassemia was found 6.3%. There was mistake at incidence so hat we improved with erratum [5]. The incidence of β-thalassemia trait was very high level, the incidence of a-thalassemia trait was also found hi...

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Spectrums of opportunistic infections in HIV-Infected patients in referral hospital of Setif (Algeria)

Results Out of 266 patients, 65% were male, the mean age was 37 years and the most frequent route of transmission was heterosexual (86%). 60 % were admitted with obvious clinical signs and symptoms, whereas 40% were asymptomatic, and they were diagnosed through screens or check-up tests. The most frequent clinical symptoms on first admission were oral candidiasis (66.4%), herpes zoster virus in...

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Epidemiological and clinical aspects of paediatric HIV infections in Setif (Algeria)

Results Of 286HIV-infected patients, 12 were children (4.1%), 8 (66.7%) of whom were male. Ages at diagnosis ranged from 6 months to 12 years (median 5). Of the 10 (83.3%) children who acquired the infection by vertical transmission, median age at diagnosis was 3 years. Only one woman was offered PMTCT interventions with HAART started lately at 38 weeks of pregnancy, oral AZT and replacement fe...

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ژورنال

عنوان ژورنال: Turkish Journal of Hematology

سال: 2010

ISSN: 1300-7777,1308-5263

DOI: 10.5152/tjh.2010.60