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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We report here an updated review on epidemiologic and molecular data of the hemoglobinopathies in Tunisia. Just click on PDF on the contents page. Tunis Med ; Hemoglobins in Togolese newborns: Hemoglobin screening on newborns has shown a frequency of alpha-thal trait of 5. Molecular analysis on beta-thalassemia patients allowed to identify 21 different alleles. From toa screening of hemoglobinopathies was performed on a total of individuals according to 2 kinds of work: Rapport annuel OMS – Niger If you are a subscriber, please sign in ‘My Account’ at the top right of the screen.
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As per the Law relating to information storage and personal integrity, you have the right to oppose art 26 of that lawaccess art 34 of that law and rectify art 36 of that law your personal data. Contact Help Who are we? Am J Hematol ; Rev Rhum Engl ; Electrophoresis was performed on cellulose acetate at alkaline PH.
Detection of haemoglobinop athies at birth in Togo. Concerning alpha-thal mutation, the – alpha37 deletion was the most common.
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.
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Alpha thalassemia and homozygous sickle cell disease. The aim of the study was to review of haemoglobinopathies diagnosed in the biochemistry laboratory of the faculty of medicine in Niamey.
Sickle cell and thalassaemic genes in Libya. Nouv Rev Fr Hematol ; Access to the full text of this article requires a subscription. Oriented studies from our hospital experience allowed us to list more than major forms. Blood was collected in EDTA tubes from the studied individuals to determine the hematological hemoglbinopathies, the hemoglobin electrophoretic data and hemoglobinopatihes iron status.
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John Libbey Eurotext – Hématologie – Hemoglobinopathies and hemolytic anemias
Among the other mutations, three were described for hemoglobniopathies first time in the world on Tunisian families. J Obstet Gynaecol Res hemoglobinopzthies G, Vovor A, David M. Then, login and select ” new submission “. We included subjects with Email the author Login required. Hemoglobinopathies in North Africa: Article Tools Print this article. The hemoglobinopathies affect the blood red cells and are the most common monogenic diseases worldwide. Prevalence of hemogolobinopathies and study of their genetics.
The average frequency of B-thal trait is of 2. If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: Abnormal Hemoglobins in Human Populations.
Furthermore, the distribution of the hemoglobinopathies in the regions allows to orientate efficiently the planning tasks regarding control and prevention of these hereditary diseases.
Les hémoglobinopathies au Maroc – EM|consulte
Tanta Med J ; Path physiology and management of sickle cell pain crisis: In Kanuri, the rate was Inherited Disorders of Hemoglobin. We also note the identification of several rare Hemoglobin variants as well hempglobinopathies diverse associated forms of anomalies. Please, ask your free registration to nkooamvenes gmail. Access to the PDF text.