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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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. Med Trop ; The average frequency of B-thal trait is of 2.

Les hémoglobinopathies au Maroc – EM|consulte

How to cite hemoglobinopathes. In Kanuri, the rate was If you are a subscriber, please sign in ‘My Account’ at the top right of the screen. Email the author Login required. Prevalence of hemoglobin S and beta-thalassemia in northern Jordan. For HbSS, the distribution in these ethnics groups was respectively Abnormal Hemoglobins in Human Populations.

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 rectify art 36 of heoglobinopathies law your personal data.

You can move this window by clicking on the headline. Detection of haemoglobinop athies at birth kes Togo. Prevalence of hemogolobinopathies and study of their genetics. Please, ask your free registration to nkooamvenes gmail. The hemoglobin S and C are the two most common haemoglobinopathies in Niger. Alpha thalassemia and homozygous sickle cell disease. DNA analysis was performed by the usual PCR based-procedures for the molecular defects identification.


Access to the text HTML. Inherited Hemoglobinopathiee of Hemoglobin. World Bank ; Contact Help Who are we? Systematic surveys allowed us to show an average prevalence of hemoglobinopathy carriers of 4. G, Vovor A, David M. Hemoglobin screening on newborns has shown a frequency of alpha-thal trait of 5.

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

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The distribution of haemoglobin C and its prevalence in newborns in Africa.

Post a Comment Login 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. Concerning alpha-thal mutation, the – alpha37 deletion was the most common. Access to the full text of this article requires a subscription.

Just click on PDF on the contents page. From toa screening of hemoglobinopathies was performed on a total of individuals according to 2 kinds of work: Hemoglobinopathies in North Africa: Tanta Med J ; Nouv Rev Fr Hematol ; Rev Rhum Engl ; Prog Clin Biol Res.


Path physiology and management of sickle cell pain crisis: Outline Masquer le plan. Hemogloginopathies this article Login required. Disease Control Priorities in Developing Countries. Sickle cell and thalassaemic genes in Libya. Top of the page – Article Outline. Article Tools Print this article.

Hemoglobins in Togolese newborns: Oriented studies from our hospital experience allowed us to list more than major forms.

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Among the other mutations, three were described for the first time in the world on Tunisian families. The hemoglobinopathies affect the blood red cells and are the most common monogenic diseases worldwide. The high frequency and clinical severity of the hemoglobinopathies, make them hemoglobinopaghies major public health problem. Rapport annuel OMS – Niger Am J Hematol ; This was a prospective and retrospective study during 10 years from to Blood was collected in EDTA pes from the studied individuals to determine the hematological parameters, the hemoglobin electrophoretic data and the iron status.