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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Tunis Med ; User Username Password Remember me. The distribution of haemoglobin C and hemoglobiopathies prevalence in newborns in Africa. Med Trop ; Detection of haemoglobinop athies at birth in Togo. Rev Rhum Engl ; You can move this window by clicking on the hemoblobinopathies.
Access to the PDF text. An updated review of the epidemiologic and molecular data. Oriented studies from our hospital experience allowed us to list more than major forms.
Sickle cell and thalassaemic genes in Libya. Disease Control Priorities in Developing Countries.
We report here an updated review on epidemiologic and molecular data of the hemoglobinopathies in Tunisia. Email this article Login required.
We also note the identification of several rare Hemoglobin variants as well as diverse associated forms of anomalies. Post a Comment Login required.
John Libbey Eurotext – Hématologie – Hemoglobinopathies and hemolytic anemias
Molecular analysis on uemoglobinopathies patients allowed to identify 21 different alleles. Prog Clin Biol Res. World Bank ; The high frequency and clinical severity of the hemoglobinopathies, make them a major public health problem. 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.
Email the author Login required. Then, login and select ” new lees “. Hemoglobin screening on newborns has shown a frequency of alpha-thal trait of 5. Outline Masquer le plan. Top of the page – Article Outline. Alpha thalassemia and homozygous sickle cell disease. DNA analysis was performed by the usual PCR based-procedures for the molecular defects identification. Prevalence of hemoglobin S and beta-thalassemia in northern Jordan.
G, Vovor A, David M.
[Hemoglobinopathies in Tunisia. An updated review of the epidemiologic and molecular data].
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. Article Tools Print this article. Just click on PDF on the contents page. Am J Hematol ; If you are a subscriber, please sign in ‘My Account’ at the top right of the screen. The average frequency of B-thal trait is of 2. If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: Contact Help Who are we?
Abnormal Hemoglobins in Human Populations. We included subjects with Tanta Med J ; Inherited Disorders of Hemoglobin.
From toa screening of hemoglobinopathies was le on a total of individuals according to 2 kinds of work: Electrophoresis was performed on cellulose acetate at alkaline PH. How to cite item. Personal information regarding our website’s visitors, including their identity, is confidential. The hemoglobin S and C are the two most common haemoglobinopathies in Niger.
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 hemoglobinopathiea art 36 of that law your personal 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. Prevalence of hemogolobinopathies bemoglobinopathies study of their genetics.
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