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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Abnormal Hemoglobins in Human Populations. Journal page Archives Contents list. 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. The aim of the study was to review of haemoglobinopathies diagnosed in the biochemistry laboratory of the faculty of medicine in Niamey. Then, login and select ” new submission “. Systematic surveys allowed us to show an average prevalence of hemoglobinopathy carriers of 4.

Molecular analysis on beta-thalassemia patients allowed to identify 21 different alleles.

You may thus request that your data, should it be inaccurate, incomplete, unclear, outdated, not be used or stored, be corrected, clarified, updated or deleted.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. We report here an updated review on epidemiologic and molecular data of the hemoglobinopathies in Tunisia.


This was a prospective and retrospective study during 10 years from to Email the author Login required. Tanta Med J ; G, Vovor A, David M.

Blood was collected in EDTA tubes from the studied individuals to determine the hematological hemoglobinipathies, the hemoglobin electrophoretic data and the iron status.


The average frequency of B-thal trait is of 2. Personal information regarding our website’s visitors, including their identity, is confidential.

In Kanuri, the rate was Top of the page – Article Outline. Access to the full text of this article requires a subscription. Tunis Med ; Concerning alpha-thal mutation, the – alpha37 deletion was the most common.

J Obstet Gynaecol Res ; Sickle cell and thalassaemic genes in Libya.

John Libbey Eurotext – Hématologie – Hemoglobinopathies and hemolytic anemias

DNA analysis was performed by the usual PCR based-procedures for the molecular defects identification. Prevalence of hemoglobin S and beta-thalassemia in northern Jordan.

Rev Rhum Engl ; Access to the PDF text. Please, ask your free registration to nkooamvenes gmail. You can move this window by clicking on the headline.

Rapport annuel OMS – Niger Access to the text HTML. Am J Hematol ; User Username Password Remember me.


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

Prevalence of hemogolobinopathies and study of their genetics. Detection of haemoglobinop athies at birth in Togo. The distribution of haemoglobin C and its prevalence in newborns in Africa. Alpha thalassemia and homozygous sickle cell disease. Hemoglobins in Togolese newborns: The hemoglobinopathies affect the hemoglobimopathies red cells and are the most common monogenic diseases worldwide.

The hemoglobin S and C are the two most common haemoglobinopathies in Niger. From toa screening of hemoglobinopathies was performed on a total of individuals according to 2 kinds of work: Hemoglobin screening on newborns has shown a frequency of alpha-thal trait of 5.

Article Tools Print this article. For HbSS, the distribution in these ethnics groups was respectively Hemoglobinopathies in North Africa: Disease Control Priorities in Developing Countries. If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: Nouv Rev Fr Hematol ; Contact Help Who are we? How to cite item. Inherited Disorders of Hemoglobin.