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.

An updated review of the epidemiologic and molecular data. Hemoglobins in Togolese newborns: Contact Help Who are we? Inherited Disorders of Hemoglobin. Hemoglobin screening on newborns has shown a frequency of alpha-thal trait of 5.

Email the author Login required. We included subjects with We also note the identification of several rare Hemoglobin variants as well as diverse associated forms of anomalies.

Tunis Med ; The high frequency and clinical severity of the hemoglobinopathies, make them a major public health problem. Just click on PDF on the contents page.

J Obstet Gynaecol Res ; User Username Password Remember me. Am J Hematol ; Access to the PDF text. This was a prospective and retrospective study during 10 years from to Post a Comment Login required.


The aim of the study was to review of haemoglobinopathies diagnosed in the biochemistry laboratory of the faculty of medicine in Niamey. World Bank ; Rapport annuel OMS – Niger For HbSS, the distribution in these ethnics groups was respectively If you are a subscriber, please sign in ‘My Account’ at the top right of the screen. Concerning alpha-thal mutation, the – alpha37 deletion was the most common.

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John Libbey Eurotext – Hématologie – Hemoglobinopathies and hemolytic anemias

Alpha thalassemia and homozygous sickle cell disease. How to cite item. Oriented studies from our hospital experience allowed us to list more than major forms.

Rev Rhum Engl ; Then, login and select ” new submission “. Top of the page – Article Outline. In Kanuri, the rate was 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. Article Tools Print this article.


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

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

Systematic surveys allowed us to show an average prevalence of hemoglobinopathy carriers of 4. G, Vovor A, David Hemoglobinopathiex. The distribution of haemoglobin C and its prevalence in newborns in Africa. We report here an updated review on epidemiologic and molecular data of the hemoglobinopathies in Tunisia.

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Disease Control Priorities in Developing Countries. Outline Masquer le plan. Hemoglobinopathies in North Africa: Furthermore, the distribution of the hemoglobinopathies in the regions allows to orientate efficiently the planning tasks regarding control and prevention of these hereditary diseases.