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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Alpha thalassemia and homozygous sickle cell disease. The hemoglobinopathies affect the blood red cells and are the most common monogenic diseases worldwide.
The hemoglobin S and C are the two most common haemoglobinopathies in Niger.
If you are a subscriber, please sign in ‘My Account’ at the top right of the screen. Rev Rhum Engl hemoglobinopathiez Inherited Disorders of Hemoglobin. Hemoglobins in Togolese newborns: 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.
Abnormal Hemoglobins in Human Populations. Contact Help Who are hempglobinopathies From toa screening of hemoglobinopathies was performed on a total of individuals according to 2 kinds of work: Post a Comment Login required.
You can move this window by clicking on the headline. If you hejoglobinopathies to subscribe to this journal, see our rates You can purchase this item in Pay Per View: DNA analysis was performed by the usual PCR based-procedures for the molecular defects identification.
Molecular analysis on beta-thalassemia patients allowed to identify 21 different alleles. Tanta Med J ; G, Vovor A, David M. Access to the PDF text.
We report here an updated review on epidemiologic and molecular data of the hemoglobinopatihes in Tunisia. Access to the text HTML. Hemoglobin screening on newborns has shown a frequency of alpha-thal trait of 5. Hemoglobinopathies in North Africa: Among the other mutations, three were described for the first time in the world on Tunisian families.
The average frequency of B-thal trait is of 2. Email this article Login required. Disease Control Priorities in Developing Countries. Prevalence of hemogolobinopathies and study of their genetics. Tunis Med ; Article Tools Print hemoglobinopsthies article.
Sickle cell and thalassaemic genes in Libya. We also note the identification of several rare Hemoglobin variants as well as diverse associated forms of anomalies.
In Kanuri, the rate was The high frequency and clinical severity of the hemoglobinopathies, make them a major public health problem. Top of the page – Article Outline. 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.
The aim of the study was to review of haemoglobinopathies diagnosed in the biochemistry laboratory of the faculty of medicine in Niamey.
This was a prospective and retrospective study during 10 years from to Furthermore, the distribution of the hemoglobinopathies in the regions allows to orientate efficiently the planning tasks regarding control and prevention of these hereditary diseases. Personal information regarding our website’s visitors, including their identity, is confidential. Then, login and select ” new submission “. We included subjects with Am J Hematol ; Nouv Rev Fr Hematol ; User Username Password Remember me.
Oriented hemoglbinopathies from our hospital experience allowed us to list more than major forms.
Access to the full text of this article requires a subscription. Journal page Archives Contents list. Hemoglobbinopathies of hemoglobin S and beta-thalassemia in northern Jordan.