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dc.contributor.authorSAFI, HAYET-
dc.date.accessioned2023-04-02T09:01:14Z-
dc.date.available2023-04-02T09:01:14Z-
dc.date.issued2017-
dc.identifier.urihttps://dspace.univ-ghardaia.edu.dz/xmlui/handle/123456789/5891-
dc.description.abstractThe present study is realized at the central laboratory of the Public Hospital of Ghardaïa, to define the biological methods for the diagnosis of sickle cell anemia (hemoglobin S), in particular hemoglobin electrophoresis. The study was on blood samples of suspected patients or in the case of family survey, 46 patients studied, whose age ranged from less than one year to 67 years, for a period of 3 months. In this period, a new case of sickle-cell anemia was founded, while in the family survey there is 8 cases of homozygous sickle-cell anemia, and 11 heterozygous sickle cell disease. The remaining 26 cases varied between patients without any pathology of hemoglobin and other hemoglobinopathy patients.EN_en
dc.language.isofrEN_en
dc.publisherFaculté Science de la Nature et de la Vie et Sciences de la Terre - Université de GhardaïaEN_en
dc.subjectDrépanocytose, hémoglobine S, électrophorèse, GhardaïaEN_en
dc.subjectSickle cell anemia, hemoglobin S, electrophoresis, GhardaïaEN_en
dc.titleMise en place des examens hématologique et de l'électrophorèse de l’hémoglobine pour le diagnostic de la drépanocytose dans la région de GhardaïaEN_en
Appears in Collections:Mémoires de Master



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