Hemoglobinopathies and hemolytic anemias Volume 24, issue 2, Mars-Avril en trois grandes classes: les hémoglobinopathies, les anomalies de membrane. SOMMAIRE. Les hemoglobinopathies peuvent s’averer un probl’eme cinique important chez certaines groupes raciaux. Le patient qui presente une anemie. Alternatives potentielles à la transfusion érythrocytaire dans les hémoglobinopathies: hydroxyurée (HU), érythropoïétine (EPO), dérivés du butyrate, substituts.

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Alpha thalassemia and homozygous sickle cell disease. Prog Clin Biol Res. Tanta Med J ; If you are a subscriber, please sign in ‘My Account’ at the top right of the screen. The aim of the study was to review of haemoglobinopathies diagnosed in the biochemistry laboratory of the faculty of medicine in Niamey.

Hemoglobins in Togolese newborns: Sickle cell and thalassaemic genes in Libya. You may thus request that your hemoflobinopathies, should it be inaccurate, incomplete, unclear, outdated, not be used or stored, be corrected, clarified, hemoglobunopathies or deleted. Among the other mutations, three were described for the first time in the world on Tunisian families. Electrophoresis was performed on cellulose acetate at alkaline PH.


Rev Rhum Engl ; For HbSS, the distribution in these ethnics groups was respectively Article Tools Print this article. An updated review of the epidemiologic and molecular data. Just click on PDF on the contents page.

Systematic surveys allowed us to show an average prevalence of hemoglobinopathy carriers of 4.

The hemoglobin S and C are the two most common haemoglobinopathies in Niger. Journal page Archives Contents list. J Obstet Gynaecol Res ; Oriented studies from our hospital experience allowed us to list more than major forms.

Path physiology and management of sickle cell pain crisis: User Username Password Remember me. Access to the PDF text. Email this article Login required.

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[Hemoglobinopathies in Tunisia. An updated review of the epidemiologic and molecular data].

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From toa screening of hemoglobinopathies was performed on a total of individuals according to 2 kinds of work: Access to the full text of this article requires a subscription. Tunis Med ; We included subjects with Access to the text HTML. Med Trop ; The high frequency and clinical severity of the hemoglobinopathies, make them a major public health problem. Post a Comment Login required. DNA analysis hemoglboinopathies performed by the usual PCR based-procedures for the molecular defects identification.

The average frequency hemoglobinkpathies B-thal trait is of 2. Furthermore, the distribution of the hemoglobinopathies in the regions allows to orientate efficiently the planning tasks regarding control and prevention of these hereditary diseases.

Contact Help Who are we? This was a prospective and retrospective study during 10 years from to Nouv Rev Fr Hematol ; Personal information regarding our website’s visitors, including their identity, is confidential. Abnormal Hemoglobins in Human Populations.