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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Hemoglobinopathies in North Africa: We included subjects with Oriented studies from our hospital experience allowed us to list more than major forms.
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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. Top of the page – Article Outline. DNA analysis was performed by the usual PCR based-procedures for the molecular defects identification. Nouv Rev Fr Hematol ; The aim of the study was to review of haemoglobinopathies diagnosed in the biochemistry laboratory of the faculty of medicine in Niamey.
Outline Masquer le plan. How to cite item. If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: Post a Comment Login required. We also note the identification of several rare Hemoglobin variants as well as diverse associated forms of anomalies.
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Prog Clin Biol Res. Abnormal Hemoglobins in Human Populations. The high frequency and clinical severity of the hemoglobinopathies, make them a major public health problem. Concerning alpha-thal mutation, the – alpha37 deletion was the most common.
Among the other mutations, three were described for the first time in the world on Tunisian families. Hemoglobins in Togolese newborns: Personal information regarding our website’s visitors, including their identity, is confidential. You can move this window by clicking on the headline. Alpha thalassemia and homozygous sickle cell disease. The owners of this website hereby guarantee to respect the legal confidentiality conditions, applicable in France, and not to disclose this data to third parties.
In Kanuri, the rate was Email this article Login required. Email the author Login required. 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 hemoylobinopathies that law your personal data. Tanta Med J ; We report hemoglobinopthies an updated review on epidemiologic and molecular data of the hemoglobinopathies in Tunisia. Rev Rhum Engl ; If you are a subscriber, please sign in ‘My Account’ at the top right of the screen.
[Hemoglobinopathies in Tunisia. An updated review of the epidemiologic and molecular data].
Sickle cell and thalassaemic genes in Libya. Systematic surveys allowed us to show an average prevalence of hemoglobinopathy carriers of 4. Detection of haemoglobinop athies at birth in Togo. Access to the text HTML.
Rapport annuel OMS – Niger This was a prospective and retrospective study during 10 years from to Tunis Med ; Access to the PDF text. Prevalence of hemogolobinopathies and study of their genetics. The hemoglobin S and C are the two most common haemoglobinopathies in Niger. Blood was collected in EDTA tubes from the studied individuals to determine the hematological parameters, the hemoglobin electrophoretic data and the iron status.
For HbSS, the distribution in these ethnics groups was respectively Hemoglobin screening on newborns has shown a frequency of alpha-thal trait of 5.
The distribution of haemoglobin C and its prevalence in newborns in Africa. Molecular hemoglobinopathis on beta-thalassemia patients allowed to identify 21 different alleles. From toa screening of hemoglobinopathies was performed on a total of individuals according to 2 kinds of work: Disease Control Priorities in Developing Countries. The hemoglobinopathies affect the blood red cells and are the most common monogenic diseases worldwide.
Just click on PDF on the heoglobinopathies page. An updated review of the epidemiologic and molecular data. 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. Article Tools Print this article.
The average frequency of B-thal trait is of 2.