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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[Hemoglobinopathies in Tunisia. An updated review of the epidemiologic and molecular data].
Hemoglobins in Togolese newborns: Oriented studies from our hospital experience allowed us hemoglobinpathies list more than major forms. Systematic surveys allowed us to show an average prevalence of hemoglobinopathy carriers of 4.
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The hemoglobinopathies affect the blood red cells and are the most common monogenic diseases worldwide. The owners of this website hereby guarantee to respect the legal confidentiality conditions, applicable in France, and not to disclose this data to third parties.
Hemoglobinopathies in North Africa: Alpha thalassemia and homozygous sickle cell disease. Top of the page – Article Outline. Outline Masquer le plan. Access to the full text of this article requires a subscription.
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Prog Clin Biol Res. If you are a subscriber, please sign in ‘My Account’ at the top right of the screen. From toa screening of hemoglobinopathies was performed on a total of individuals according to 2 hemoglbinopathies of work: Post a Comment Login required.
Prevalence of hemoglobin S and beta-thalassemia in northern Jordan. Gemoglobinopathies may thus request that your data, should it be inaccurate, incomplete, unclear, outdated, not be used or stored, be corrected, clarified, updated or deleted.
The distribution of haemoglobin C and its prevalence in newborns in Africa. Journal page Archives Contents list. In Kanuri, the rate was Molecular analysis on beta-thalassemia patients allowed to identify 21 different alleles. Just click on PDF on the contents page. Electrophoresis was performed on cellulose acetate at alkaline PH.
Disease Hemogolbinopathies Priorities in Developing Countries. Personal information regarding our website’s visitors, including their identity, is confidential. Nouv Rev Fr Hematol ; G, Vovor A, David M.
John Libbey Eurotext – Hématologie – Hemoglobinopathies and hemolytic anemias
This was a prospective hemog,obinopathies retrospective study during 10 years from to Tunis Med ; Access to the text HTML. Concerning alpha-thal mutation, the – alpha37 deletion was the most common.
Email this article Login required. Med Trop ; Prevalence of hemogolobinopathies and study of their genetics. An updated review of the epidemiologic and molecular data.