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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Prevalence of hemoglobin S and beta-thalassemia in northern Jordan. J Obstet Gynaecol Res ; Oriented studies from our hospital hemoglibinopathies allowed us to list more than major forms. Just click on PDF on the contents page. Disease Control Priorities in Developing Countries. Path physiology and management of sickle cell pain crisis: Hemoglobionpathies also note the identification of several rare Hemoglobin variants as well as diverse associated forms of anomalies.

We included subjects with Abnormal Hemoglobins in Human Populations. Access to the text HTML.

Med Trop ; G, Vovor A, David M. 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.


Les hémoglobinopathies au Maroc – EM|consulte

Rev Rhum Engl ; Journal page Archives Contents list. Molecular analysis on beta-thalassemia patients allowed to identify 21 different alleles.

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

Rapport annuel OMS – Niger Concerning alpha-thal mutation, the – alpha37 deletion was the most common. Access to the full text of this article requires a subscription. Alpha thalassemia and homozygous sickle cell disease. If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: Top of the page – Article Outline.

From toa screening of hemoglobinopathies was performed on a total of individuals according to 2 kinds of work: The aim of the study was to review of haemoglobinopathies diagnosed in the biochemistry laboratory of the faculty of medicine in Niamey.

This was a prospective and retrospective study during 10 years from to Email the author Login required. Email this article Login required. Nouv Rev Fr Hematol ; Among the other mutations, three were described for the first time in the world on Tunisian families. We report here an updated review on epidemiologic and molecular data of the hemoglobinopathies in Tunisia.


Sickle cell and thalassaemic genes in Libya.

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

World Bank ; The hemoglobin S and C are the two most common haemoglobinopathies in Niger. Hemoglobins in Togolese newborns: Electrophoresis was performed on cellulose acetate at alkaline PH. If you are a subscriber, please sign in ‘My Account’ at the top right of the screen. The average frequency of B-thal trait is of 2.

Then, login and hemoglobinopatbies ” new submission “. Article Tools Print this article. Blood was collected in EDTA tubes from the studied individuals to determine the hematological parameters, the hemoglobin electrophoretic data and the iron status.


Hemoglobinopathies in North Africa: How to cite item. The high frequency and clinical severity of the hemoglobinopathies, make them a major public health problem. The hemoglobinopathies affect the blood red cells and are the most common monogenic diseases worldwide.