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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The MRI appearance of marrow is a reflection of transfusion and chelation therapy. Access to the full text of this article requires a subscription. Other complications include growth retardation, bone deformation and marrow hyperplasia which are avoided by regular blood transfusion.
In all types of thalassemia, clinical features that result from anemia, transfusional, and absorptive iron overload are similar but vary in severity. Access to the text HTML. If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: You may thus request that your data, should it be inaccurate, incomplete, unclear, outdated, not be used or stored, be corrected, clarified, updated or deleted.
The skeletal X-ray findings show characteristies of chronic overactivity of the marrow. The hematologic findings were similar to those reported in the past in other populations. Top of the page – Article Outline. If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: If you are a subscriber, please sign in ‘My Account’ at the top right of the screen. Open in a separate window. J Lab Clin Med.
Orphanet: Diagnostic moleculaire de la thalassemie alpha genes HBA1 HBA2
ThalassemiaImagingBone. Access to the text HTML. Support Center Support Center. Thalassemia is a chronic, inherited microcyric anemia characterized by defective hemoglobin synthesis.
Annales de Biologie Clinique
Associated Data Supplementary Materials. Access to the Thalaasemie text. You may thus request that your data, should it be inaccurate, incomplete, unclear, outdated, not be used or stored, be corrected, clarified, updated or deleted. This article has been cited by other articles in PMC.
Homozygous hhalassemie is a severe, transfusion dependent anaemia that also causes infertility. 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.
This is the first report of such a number of cases of beta-thalassemia in this population.
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. Very few pregnancies are reported among such patients. Thalassaemia in the British.
Two cases of delta beta-thalassemia minor in sisters are also reported; this is the first thalassejie of such cases in French Canadians. Valetand P. Personal information regarding our website’s visitors, including their identity, is confidential.
Beta-thalassemia major ; Infertility ; Pregnancy ; Anesthesia ; Preimplantation genetic diagnosis. Haematological data in cases of -thalassaemia trait in Thailand.
La thalassémie chez les Québécois francophones.
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Estimation of small percentages of foetal haemoglobin. Outline Masquer le plan. Preimplantation genetic diagnosis is possible. If you are a subscriber, please sign in ‘My Account’ at the top right of the screen. Most of the families had settled in Quebec thalassemmie than years ago, largely in Portneuf county.