la β-thalassémie intermédiaire avec des besoins transfusionnels Certaines thalassémies intermédiaires ont un taux d’hémoglobine bas de façon prolongée. Abstract. Eighty-five cases of beta-thalassemia minor were found between January and November in 18 families of. Département d’Hématologie biologique; CHU de Montpellier – Hôpital Saint-Eloi; 80 avenue Augustin Fliche; MONTPELLIER CEDEX 5; FRANCE.
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Thus, beta-thalassemia minor is a relatively common condition in Quebec and must be considered in cases of microcytic anemia without evidence of iron deficiency.
La thalassémie chez les Québécois francophones.
Thalassemia is a chronic, inherited microcyric anemia characterized by defective hemoglobin synthesis. 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. If you want to subscribe to this journal, see our rates You can purchase this item laa Pay Per View: Outline Masquer le plan. Thalassaemia in the British. Personal information regarding our website’s visitors, including their identity, is confidential.
Other complications include growth retardation, bone deformation and marrow hyperplasia which are avoided by regular blood transfusion.
This is the first report of such a number of cases of beta-thalassemia in this population. 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.
Orphanet: Diagnostic moleculaire de la thalassemie alpha genes HBA1 HBA2
Contact Help Who are we? Estimation of small percentages of foetal haemoglobin. Homozygous beta-thalassemia is a severe, transfusion dependent anaemia that also causes infertility. Open in a separate window.
Annales de Biologie Clinique
Access to the text HTML. Haematological data in cases of -thalassaemia trait in Thailand.
Most of the families had settled in Quebec more than years ago, largely in Portneuf county. Access to the text HTML. Top of the page – Article Outline. The MRI appearance of marrow is a reflection of transfusion and chelation therapy. 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.
Glycerol lysis time as a screening test for erythrocyte disorders. Journal page Archives Contents list. They have a very high obstetrical risk and a rhalassemie follow is necessary. You can move this window by clicking on the headline.
As per the Law relating to information storage and personal integrity, you have the right to oppose art 26 of that lawaccess thaalssemie 34 of that law and rectify art 36 of that law your personal data.
Access to the full text of this article requires a subscription. The skeletal X-ray findings show characteristies of chronic overactivity of the marrow. National Center for Biotechnology InformationU. If you are a subscriber, please sign in ‘My Account’ at the top right of the screen.
Orphanet: Diagnostic moleculaire de la thalassemie delta gene HBD
Very few pregnancies are reported among such patients. Personal information regarding our website’s visitors, including their identity, is confidential.
Valetand P. You can move this window by clicking on the headline.
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