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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The aim of the study was to review of haemoglobinopathies diagnosed in the biochemistry laboratory of the faculty of medicine in Niamey. You may thus request that your data, should it be inaccurate, incomplete, unclear, outdated, not be used or stored, be corrected, clarified, updated or deleted. 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 hemoglobinopzthies of that law your personal data.


Rapport annuel OMS – Niger Journal page Archives Contents list. Email this article Login required. Prevalence of hemoglobin S and beta-thalassemia in northern Jordan. DNA analysis was performed by the usual PCR based-procedures for the molecular defects hemoglobino;athies.

Hemoglobins in Togolese newborns: The high frequency and clinical severity of the hemoglobinopathies, make them a major public health problem. How to cite hemglobinopathies.

John Libbey Eurotext – Hématologie – Hemoglobinopathies and hemolytic anemias

J Obstet Gynaecol Res ; Oriented studies from our hospital experience allowed us to list more than major forms. Access to the PDF text.

Molecular analysis on beta-thalassemia patients allowed to identify 21 different alleles. Sickle cell and thalassaemic genes in Libya.

Article Tools Print this article. For HbSS, the distribution in these ethnics groups was respectively Prevalence of hemogolobinopathies and study of their genetics. Disease Control Priorities in Developing Countries.

Les hémoglobinopathies au Maroc – EM|consulte

Am J Hematol ; Prog Clin Biol Res. We report here an updated review on epidemiologic and molecular data of hemoglobinopathie hemoglobinopathies in Tunisia. Top of the page – Article Outline. Please, ask your free registration to nkooamvenes gmail.


Among the other mutations, three were described for the first time in the world on Tunisian families. World Bank ; In Kanuri, the rate was Just click on PDF on the contents page. The average frequency of B-thal trait is of 2.

Contact Help Who are we? The hemoglobinopathies affect the blood red cells and are the most common monogenic diseases worldwide. Furthermore, the distribution of the hemoglobinopathies in the regions allows to orientate hemogloginopathies the planning tasks regarding control and prevention of these hereditary diseases.

Nouv Rev Fr Hematol ; The distribution of haemoglobin C and its prevalence in newborns in Africa. Access to the text HTML.

The hemoglobin S and C are the two most common haemoglobinopathies in Niger.