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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Rapport annuel OMS – Niger Path physiology and management of sickle cell pain crisis: Then, login and select ” new submission “. Detection of haemoglobinop athies at birth in Togo. Article Tools Print this article. Access to the PDF text.
John Libbey Eurotext – Hématologie – Hemoglobinopathies and hemolytic anemias
Systematic surveys allowed us to show an average prevalence of hemoglobinopathy carriers of 4. Access to the full text of this article requires a subscription. The aim of the study was to review of haemoglobinopathies diagnosed in the biochemistry laboratory of pes faculty of medicine in Niamey. The high frequency and clinical severity of the hemoglobinopathies, make them a major public health problem. How to cite item.
Blood was collected in EDTA tubes from the studied hemotlobinopathies to determine the hematological parameters, the hemoglobin electrophoretic data and the iron hemoglobinopatnies. Email this article Login required. Among the other mutations, three were described for the first time in the world on Tunisian families. DNA analysis was performed by the usual PCR based-procedures for the molecular defects identification.
Sickle cell and thalassaemic genes in Libya. The hemoglobin S and C are the two most common haemoglobinopathies in Niger. 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. Oriented studies from our hospital experience allowed us to list more than hemohlobinopathies forms.
Hemoglobihopathies report here an updated review on epidemiologic and hemogglobinopathies data of the hemoglobinopathies in Tunisia. Inherited Disorders of Hemoglobin.
Access to the text HTML. Med Trop ; We also note the identification of several rare Hemoglobin variants as well as diverse associated forms of anomalies. Tunis Med ; Email the author Login required. Top of the page – Article Outline. Disease Control Priorities in Developing Countries. Rev Rhum Engl ; Outline Masquer le plan. Tanta Med J ; In Kanuri, the rate was Abnormal Hemoglobins in Human Populations.
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[Hemoglobinopathies in Tunisia. An updated review of the epidemiologic and molecular data].
Just click on PDF on the contents page. Prog Clin Biol Res.
Prevalence of hemogolobinopathies and study of their genetics. Personal information regarding our website’s visitors, including their identity, is confidential. For HbSS, the distribution in these hemoglobinopaties groups was respectively Hemoglobin screening on newborns has shown a frequency of alpha-thal trait of 5.
J Obstet Gynaecol Res ; The hemoglobinopathies affect the blood red cells and are the most common monogenic diseases worldwide.
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Am J Hematol ; If you are a subscriber, please sign in ‘My Account’ at the top right of the screen. Post a Comment Login required. The distribution of haemoglobin C and its prevalence in newborns in Africa. This was a prospective and retrospective study during 10 years from to Electrophoresis was performed on cellulose acetate at alkaline PH. An updated review of the epidemiologic and molecular data. Journal page Archives Contents list. If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: