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.

Author: Kigal Meztimi
Country: Burkina Faso
Language: English (Spanish)
Genre: Life
Published (Last): 3 March 2007
Pages: 179
PDF File Size: 18.43 Mb
ePub File Size: 1.46 Mb
ISBN: 448-1-91201-563-3
Downloads: 9651
Price: Free* [*Free Regsitration Required]
Uploader: Moogumuro

An updated review of the epidemiologic and molecular data. Oriented studies from our hospital experience allowed us to list more than major forms.

John Libbey Eurotext – Hématologie – Hemoglobinopathies and hemolytic anemias

Access to the text Hemog,obinopathies. Sickle cell and thalassaemic genes in Libya. We report here an updated review on epidemiologic and molecular data of the hemoglobinopathies in Tunisia.

Am J Hematol ; Nouv Rev Fr Hematol ; You may thus request that your heomglobinopathies, should it be inaccurate, incomplete, unclear, outdated, not be used or stored, be corrected, clarified, updated or deleted. Then, login and select ” new submission “. Email this article Login required. The hemoglobinopathies affect the blood red cells and are the most common monogenic diseases worldwide.


This was a prospective and retrospective study during 10 years from to Alpha thalassemia and homozygous sickle cell disease. 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. Electrophoresis was performed on cellulose acetate at alkaline PH. The distribution of haemoglobin C and its prevalence in newborns in Africa. Personal information regarding our website’s visitors, including their identity, is confidential.

Detection of haemoglobinop athies at birth in Togo. We included subjects with The aim of the study was to review of haemoglobinopathies diagnosed in the biochemistry laboratory of the faculty of medicine in Niamey. Journal page Archives Contents list.


Contact Help Who are we? 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 that law your personal data.

User Username Password Remember me. Just click on PDF on the contents page.


Furthermore, the distribution of the hemoglobinopathies in the regions allows to orientate efficiently the planning tasks regarding control and prevention of these hereditary diseases.

Med Trop ; The hemoglobin S and C are the two most common haemoglobinopathies in Niger. Path physiology and management of sickle cell pain crisis: Access to the PDF text.

How to cite item. Abnormal Hemoglobins in Human Populations. Concerning alpha-thal mutation, the – alpha37 deletion was the most common. We also note the identification of several rare Hemoglobin variants as well as diverse associated forms of anomalies. Tunis Med ; From toa screening of hemoglobinopathies was performed on a total of individuals according to 2 kinds of work: In Kanuri, the rate was For HbSS, the distribution in these ethnics groups was respectively G, Vovor A, David M.

Among the other mutations, three were described for the first time in the world on Tunisian families.