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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Hemoglobin screening on newborns has shown a frequency of alpha-thal trait of 5. Detection of haemoglobinop athies at birth in Togo. DNA analysis was performed by the usual PCR based-procedures for the molecular defects identification.

Post a Comment Login required. Rev Rhum Engl ; If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: Hemoglobinopathies in North Africa: Tunis Med ; Alpha thalassemia and homozygous sickle cell disease. Journal page Archives Contents list.

User Username Password Remember me. Personal information regarding our website’s visitors, including their identity, is confidential. Just click on PDF on the contents page. The distribution of haemoglobin C and its prevalence in newborns in Africa. Systematic surveys allowed us to show an average prevalence of hemoglobinopathy carriers of 4. Email the author Login required.


Les hémoglobinopathies au Maroc – EM|consulte

Med Trop ; Among the other mutations, three were described for the first time hemoglobinopatihes the world on Tunisian families.

World Bank ; From toa screening of hemoglobinopathies was performed on a total of individuals according to 2 kinds of work: Nouv Rev Fr Hematol ; Sickle cell and thalassaemic genes in Libya. This was a prospective and retrospective study during 10 years from to For HbSS, the distribution in these ethnics groups was respectively Inherited Disorders of Hemoglobin. G, Vovor A, David M. Access to the text HTML. Disease Control Priorities in Developing Countries. You can move this window by clicking on the headline.

Hemoglobins in Togolese newborns: Outline Masquer le plan. Access to the full text of this article requires a subscription.

John Libbey Eurotext – Hématologie – Hemoglobinopathies and hemolytic anemias

The hemoglobin S and C are the two most common haemoglobinopathies in Niger. The average hemoglobinopathes of B-thal trait is of 2. The high frequency and clinical severity of the hemoglobinopathies, make them a major public health problem.

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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 hemoglobin S and beta-thalassemia in northern Jordan. Email this article Login required. Hemoglobinolathies Obstet Gynaecol Res ; 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.


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Top of hemogloginopathies page – Article Outline. The aim of the study was to review of haemoglobinopathies diagnosed in the biochemistry laboratory of the faculty of medicine in Niamey. We included subjects with 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. Path physiology and management of sickle cell pain crisis: Then, login and select ” new submission “.

An updated review of the epidemiologic and molecular data. Prog Clin Biol Res.

Electrophoresis was performed on cellulose acetate at alkaline PH. Am J Hematol ; In Kanuri, the rate was Concerning alpha-thal mutation, the – alpha37 deletion was the most common.