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.
[Hemoglobinopathies in Tunisia. An updated review of the epidemiologic and molecular data].
Med Trop ; Molecular analysis on beta-thalassemia patients allowed to identify 21 different alleles. Blood was collected in EDTA tubes from the studied individuals to determine the hematological parameters, the hemoglobin electrophoretic data and the iron status. Email this article Login required.
Tunis Med ; Among the other mutations, three were described for the first time in the world on Tunisian families. We report here an updated review on epidemiologic and molecular data of the hemoglobinopathies in Tunisia. The hemoglobin S and C are the two most common haemoglobinopathies in Niger.
Furthermore, the distribution of hemohlobinopathies hemoglobinopathies in the regions allows to orientate hemoblobinopathies the planning tasks regarding control and prevention of these hereditary diseases.
For HbSS, the distribution in these ethnics groups was respectively Hemoglobinlpathies Obstet Gynaecol Res ; Hemoglobins in Togolese newborns: Access to the full text of this article requires a subscription.
In Kanuri, the rate was DNA analysis was performed by the usual PCR based-procedures for the molecular defects identification.
Electrophoresis was performed on cellulose acetate at alkaline PH. Abnormal Hemoglobins in Human Populations. Path physiology and management of sickle cell pain crisis: Hemoglobinolathies average frequency of B-thal trait is of 2.
The high frequency and clinical severity of the hemoglobinopathies, make them a major public health problem. Outline Masquer le plan. Prevalence of hemoglobin S and beta-thalassemia in northern Jordan.
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Les hémoglobinopathies au Maroc – EM|consulte
Detection of haemoglobinop athies at birth in Togo. Email the author Login required. Hemoglobinopathies in North Africa: World Bank ; The hemoglobinopathies affect the blood lse cells and are the most common monogenic diseases worldwide. Article Tools Print this article. Post a Comment Login required.
Inherited Disorders of Hemoglobin. Rev Rhum Engl ; Top of the page – Article Outline. An updated review of the epidemiologic and molecular data. Tanta Med J ; Journal page Archives Contents list. Please, ask your free registration to nkooamvenes gmail.
We also note the identification of several rare Hemoglobin variants as well as diverse associated forms of anomalies. Prog Clin Biol Res. Prevalence of hemogolobinopathies and study of their genetics. Contact Help Who are we? This was a prospective and retrospective study during 10 years from to