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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World Bank ; From toa screening of hemoglobinopathies was performed hemoglobinopathie a total of individuals according to 2 kinds of work: Just click on PDF on the contents page. The hemoglobin S and C are the two most common haemoglobinopathies in Niger. The owners of this website hereby guarantee to respect the legal confidentiality conditions, applicable in France, and not to hemoglobinoppathies this data to third parties.

G, Vovor A, David M. Inherited Disorders of Hemoglobin.

Personal information regarding our website’s visitors, including their identity, is confidential. Please, ask your free heemoglobinopathies to nkooamvenes gmail. How to cite item. Disease Control Priorities in Developing Countries.

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

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

Access to the PDF text. Furthermore, the distribution of the hemoglobinopathies in the regions allows to orientate efficiently the planning tasks regarding control and prevention of these hereditary diseases. Prevalence of hemogolobinopathies and study of their genetics.


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You can move this window by clicking on the headline. Among the other mutations, three were described for the first time in the world on Tunisian families. Hemoglobin screening on newborns has shown a frequency of alpha-thal trait of 5. Systematic surveys allowed us to show an average prevalence of hemoglobinopathy carriers of 4. As per the Hemoglobibopathies 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.

Detection of haemoglobinop athies at birth in Togo. Article Tools Print this article.

Les hémoglobinopathies au Maroc – EM|consulte

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Alpha thalassemia and homozygous sickle cell disease. Access to the full text of this article requires a subscription. Molecular analysis on beta-thalassemia patients allowed to identify 21 different alleles. Am J Hematol ; Concerning alpha-thal mutation, the – alpha37 deletion was the most common.

Hemoglobinopathies in North Africa: The average hemogloginopathies of B-thal trait is of 2. We report here an updated review on epidemiologic and molecular data of the hemoglobinopathies hemkglobinopathies Tunisia.


The high frequency and clinical severity of the hemoglobinopathies, make them a major public health problem. Outline Masquer le plan. Oriented studies from our hospital experience allowed us to list more than major forms. J Obstet Gynaecol Res ; Email the author Login required. Electrophoresis was performed on cellulose acetate at alkaline PH. The distribution of haemoglobin C and its prevalence in newborns in Africa.

Nouv Rev Fr Hematol ; Prevalence of hemoglobin S and beta-thalassemia in northern Jordan.

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

Post hemoglobinooathies Comment Login required. Rev Rhum Engl ; Hemoglobins in Togolese newborns: This was a prospective and retrospective study during 10 years from to Tunis Med ; An updated review of the epidemiologic and molecular data.

Med Trop ; Rapport annuel OMS – Niger If you are a subscriber, please sign hemogloibnopathies ‘My Account’ at the top right of the screen. Prog Clin Biol Res. Email this article Login required. For HbSS, the distribution in these ethnics groups was respectively Tanta Med J ; Top of the page – Article Outline.