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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The high frequency and clinical severity of the hemoglobinopathies, make them a major public health problem. Prevalence of hemogolobinopathies and study of their genetics.
[Hemoglobinopathies in Tunisia. An updated review of the epidemiologic and molecular data].
From toa screening of hemoglobinopathies was performed on a total of individuals according to 2 kinds of work: In Kanuri, the rate was You can move this window by clicking on the headline. Then, login and select hemoglohinopathies new submission “. Abnormal Hemoglobins in Human Populations. For HbSS, the distribution in these ethnics groups was respectively The owners of this website hereby guarantee to respect the legal confidentiality conditions, applicable in France, and not hemoglobinopathis disclose this data to third parties.
Please, ask your free registration to nkooamvenes gmail. Electrophoresis was performed on cellulose acetate at alkaline PH. Tanta Med J ; Prog Clin Biol Res.
Top of the page – Article Outline. Email this article Login required. Blood was collected in EDTA tubes from the studied individuals to determine the hematological parameters, the hemoglobin electrophoretic data and the iron status.
DNA analysis was performed by the usual PCR based-procedures for the molecular defects identification. Hemoglobin screening on newborns has shown a frequency of alpha-thal trait of 5. Path physiology and management of sickle cell pain crisis: Hemoglobinopathies in North Africa: The average frequency of B-thal trait is of 2.
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Sickle cell and thalassaemic genes in Libya. How to cite item.
The hemoglobinopathies affect the blood red cells and are the most common monogenic diseases worldwide. You may thus request that your data, should it be inaccurate, incomplete, unclear, outdated, not be used or stored, be corrected, clarified, updated or deleted. If you are a subscriber, please sign in ‘My Account’ at the top right of the screen.
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We also note the identification of several rare Hemoglobin variants as well as diverse associated forms of anomalies. J Obstet Gynaecol Res ; We included subjects with G, Vovor A, David M. World Bank ; Access to the full text of this article requires a subscription. Prevalence of hemoglobin S and beta-thalassemia in northern Jordan. User Username Password Remember me.
Molecular analysis on beta-thalassemia patients allowed to identify 21 different alleles. The aim of the study was to review less haemoglobinopathies diagnosed in the biochemistry laboratory of the faculty of medicine in Niamey.