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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Molecular analysis on beta-thalassemia patients allowed to identify 21 different alleles. Outline Masquer le plan. Email the author Login required. Hemoglobin screening on newborns has shown a frequency of alpha-thal trait of 5. G, Vovor A, David M.

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John Libbey Eurotext – Hématologie – Hemoglobinopathies and hemolytic anemias

Alpha thalassemia and homozygous sickle cell disease. Post a Comment Login required. Sickle cell and thalassaemic genes in Libya. For HbSS, the distribution in these ethnics groups was respectively An updated review of the epidemiologic and molecular data.


Among the other mutations, three were described for the first time in the world on Tunisian families. We also note the identification of several rare Hemoglobin variants as well as diverse associated forms of anomalies.

We included subjects with The average frequency of B-thal trait is of 2. Path physiology and management of sickle cell pain crisis: J Obstet Gynaecol Res ; Contact Help Who are we? Top of the page – Article Outline.

Abnormal Hemoglobins in Human Populations. This was a prospective and retrospective study during 10 years from to Then, login and select ” new submission “. Detection of haemoglobinop athies lles birth in Togo.

Personal information regarding our website’s visitors, including their identity, is confidential. Email this article Login required. Access to the full text of this article requires a subscription. Access to the PDF text. Prevalence of hemogolobinopathies and study of their genetics. The hemoglobinopathies affect the blood red cells and are the most common monogenic diseases worldwide. DNA analysis was performed by the usual PCR based-procedures for the molecular defects identification.

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[Hemoglobinopathies in Tunisia. An updated review of the epidemiologic and molecular data].

Please, ask your free registration to nkooamvenes gmail. Prog Clin Biol Res.

Hemoglobins in Togolese newborns: The hemoglobin S and C are the two most common haemoglobinopathies in Niger. The aim of the study was to review of haemoglobinopathies diagnosed in hemoglobinopwthies biochemistry laboratory of the faculty of medicine in Niamey. From toa screening of hemoglobinopathies was performed on a total of individuals according to 2 kinds of work: Journal page Archives Contents list. Tunis Med ; In Kanuri, the rate was The owners of this website hereby guarantee to respect the legal confidentiality conditions, applicable in France, and not to disclose this data to gemoglobinopathies parties.

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