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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John Libbey Eurotext – Hématologie – Hemoglobinopathies and hemolytic anemias

Then, login and select ” new submission “. Access to the PDF text. Electrophoresis was performed on cellulose acetate at alkaline PH. Hemoglobinopathies in North Africa: You can move this window by clicking on hemogloobinopathies headline.

Access to the full text of this article requires nemoglobinopathies subscription. You may thus request that your data, should it be inaccurate, incomplete, unclear, outdated, not be used or stored, be corrected, clarified, updated or deleted. Prog Clin Biol Res. Concerning alpha-thal mutation, the – alpha37 deletion was the most common.


Molecular analysis on beta-thalassemia patients allowed to identify 21 different alleles. Email the author Login required. Access to the text HTML. Article Tools Print this article. Detection of haemoglobinop athies at birth in Togo.


The average frequency of B-thal trait is of 2. Contact Help Who are we? Hemoglobins in Togolese newborns: Tanta Med J ; Journal page Archives Contents list.

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

Top of the page – Article Outline. Oriented studies from our hospital experience allowed us to list more than major forms. This was a prospective and retrospective study during 10 years from to From toa screening of hemoglobinopathies was performed on a total of individuals according to 2 kinds of hemoglpbinopathies Among the other mutations, three were described for the first time in the world on Tunisian families. DNA analysis was performed by the usual PCR based-procedures for the molecular defects identification.

Abnormal Hemoglobins in Human Populations. Systematic surveys allowed us to show an average prevalence of hemoglobinopathy carriers of 4. The hemoglobinopathies affect the blood red cells and are the most common monogenic diseases worldwide.

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

If you are a subscriber, please sign in ‘My Account’ at the top right of the screen. For HbSS, the distribution in these ethnics groups was respectively Email this article Login required. Furthermore, the distribution of the hemoglobinopathies in the regions allows to orientate efficiently the planning tasks regarding control and prevention of these hereditary diseases.


Rev Rhum Engl ; 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.

In Kanuri, the rate was Just click on PDF on the contents page. Outline Masquer le plan. Am J Hematol ; Path physiology and management of sickle cell pain crisis: Please, ask your free registration to hemoglbinopathies gmail. We report here an updated review on epidemiologic and molecular data of the hemoglobinopathies in Tunisia.

Tunis Med ; How to cite item. World Bank ; 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.

Personal information regarding our website’s visitors, including their identity, is confidential. An updated review of the epidemiologic and molecular data. G, Vovor A, David M. Prevalence of hemogolobinopathies and study of their genetics. If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: