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.
|Published (Last):||21 August 2008|
|PDF File Size:||12.37 Mb|
|ePub File Size:||3.8 Mb|
|Price:||Free* [*Free Regsitration Required]|
Furthermore, the distribution of the hemoglobinopathies in the regions allows to orientate efficiently the planning tasks regarding control and prevention of these hereditary diseases.
Electrophoresis was performed on cellulose acetate at alkaline PH. Please, ask your free registration to nkooamvenes gmail. Prog Clin Biol Res. Abnormal Hemoglobins in Human Populations. User Username Password Remember me.
Hemoglobin screening on newborns has shown a frequency of alpha-thal trait of 5. Hemoglobnopathies click on PDF on the contents page. Detection of haemoglobinop athies at birth in Togo.
The aim of the study was to review of haemoglobinopathies diagnosed in the biochemistry laboratory of the faculty of medicine in Niamey. Tunis Med ; DNA analysis was performed by the usual PCR based-procedures for the molecular defects identification. Alpha thalassemia and homozygous sickle cell disease. Email the author Login required. Path physiology and management of sickle cell pain crisis: Inherited Disorders of Hemoglobin.
The distribution of haemoglobin C and its prevalence in hemogloninopathies in Africa. Rapport annuel OMS – Niger Personal information regarding our website’s visitors, including their identity, is confidential. Blood was collected in EDTA tubes from the studied individuals to determine the hematological parameters, the hemoglobin electrophoretic data and the iron status. Among the other mutations, three were described for the first time in the world on Tunisian families.
Top of the page – Article Outline.
Email this article Login required. Post a Comment Login required. An updated review of the epidemiologic and molecular data.
You can move this window by clicking on the headline. Prevalence of hemogolobinopathies and study of their genetics. Hemoglobins in Togolese newborns: Then, login and select ” new submission “. We also note the identification of several rare Hemoglobin variants as well as diverse associated forms of anomalies.
We included subjects with J Obstet Gynaecol Res ; Outline Masquer le plan. This was a prospective and retrospective study during 10 hemoglobinopathkes from to Rev Rhum Engl ; World Bank ; The hemoglobinopathies affect the blood red cells and are the most common monogenic diseases worldwide.
G, Vovor A, David M. The hemoglobin S and C are the two most common haemoglobinopathies in Niger.
For HbSS, the distribution in these ethnics groups was respectively Oriented studies from our hospital experience allowed us to list more than major forms. Molecular analysis on beta-thalassemia patients allowed to identify 21 different alleles.
Les hémoglobinopathies au Maroc – EM|consulte
If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: Med Trop ; How to cite item. From toa screening of hemoglobinopathies was performed on a total of individuals according to 2 kinds of work: Sickle cell and hemglobinopathies genes in Libya.
Systematic surveys allowed us to show an average prevalence of hemoglobinopathy carriers of 4. Tanta Med J ; Hemoglobinopathies in North Africa: We report here an updated review on epidemiologic and molecular data of the hemoglobinopathies in Tunisia. Am J Hematol ; Journal page Archives Contents list. Access to the full text of this article requires a subscription.
The owners of this website hereby guarantee to respect the legal hemoglobinlpathies conditions, hemogpobinopathies in France, and not to disclose this data to third parties.
Prevalence of hemoglobin S and beta-thalassemia in northern Jordan.