LA THALASSEMIE PDF

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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Preimplantation genetic diagnosis is possible. Very few pregnancies are reported among such patients. 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.

You can move this window by clicking on the headline. They have a very high obstetrical risk and a pluridiscplinary follow is necessary. This is the first report of such a number of cases of beta-thalassemia in thalasswmie population.

Homozygous beta-thalassemia is a severe, transfusion dependent anaemia that also causes infertility. Personal information regarding our website’s visitors, including their identity, is confidential.

Eighty-five cases of beta-thalassemia minor were found between January and November in 18 families of French-speaking Quebeckers without Mediterranean ancestry.

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purchase this item in Pay Per View: You may thus request that your data, should it be inaccurate, incomplete, unclear, outdated, not be used or stored, be corrected, thalzssemie, updated or deleted. Copyright and License information Disclaimer. Access to the fhalassemie text of this article requires a subscription.

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Associated Data Supplementary Materials. Abstract Eighty-five cases of beta-thalassemia minor were found between January and November in 18 families of French-speaking Quebeckers without Mediterranean ancestry.

If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: Access to the full text of this article requires a subscription. As per thalasssmie 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. Thalassemia is a chronic, inherited microcyric anemia characterized by defective hemoglobin synthesis.

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Thalassémie alpha liée à l’X avec retard mental

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La thalassémie chez les Québécois francophones.

Other complications include growth retardation, bone deformation and marrow hyperplasia which are avoided by regular blood transfusion. Please review our privacy policy. Personal information regarding our website’s visitors, including their identity, is confidential. You can move this window by clicking on the headline.

Thalassémie alpha liée à l’X avec retard mental — Wikipédia

Thalassaemia in the British. 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. 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.

Access to the text HTML. Contact Help Who are we? The hematologic findings were similar to those reported in the past in other populations.

You may thus request that your data, should it be inaccurate, incomplete, unclear, outdated, not be used or stored, be thalassejie, clarified, updated or deleted.