Dans la ß-thalassémie majeure ou anémie de Cooley, l’hémoglobine A, tétramère a2b2, est synthétisée en quantité extrêmement réduite voire nulle. 21 – N° 6 – p. – Profil clinico-biologique et immunohématologique des patients atteints de?-thalassémie en Tunisie: à propos de 26 cas – EM|consulte. Vox Sang. Jul-Aug;10(4) Transfusion reaction during marrow suppression in a thalassemie patient with blood group anomaly and an unusual cold.

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thalassémie – English translation – Linguee

Adverse effects are primary skin thalasemie around the injection site and hearing loss. Archived from the original on Bone marrow deficiency diseases caused by abnormal red blood cell [ Hereditary spherocytosis Minkowski—Chauffard syndrome Hereditary elliptocytosis Southeast Asian ovalocytosis Hereditary stomatocytosis. It was coined because the condition called “Mediterranean anemia” was first described in people of Mediterranean ethnicities.

American Society of Health-System Pharmacists. People with severe thalassemia require medical treatment. Thalasseime Clinical Hematology Gene therapy is being studied for thalassemia. Thalassemias are particularly associated with people of Mediterranean origin, Arabs especially Palestinians and people of Palestinian descentand Asians.

The beta form of thalassemia is particularly prevalent talassemie Mediterranean peoples, and this geographical association is responsible for its original name. Writing tools A collection of writing tools that cover the many facets of English and French grammar, style and usage.


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Archived from the original on 15 September Large scale awareness campaigns are being organized in India [30] both by government and non-government organizations in favor of voluntary premarital screening to detect carriers of thalassemia and marriage between both carriers are strongly discouraged. Indian Journal of Endocrinology and Metabolism.

After destroying the affected person’s bone marrow with a dose of chemotherapy a myeloablative conditioning regimenthe altered HSCs are infused back into the affected person where they become engrafted in the bone marrow where they proliferate.

The cost is also significant. Archived from the original on 16 September Thalassemias also occur in descendants of people from Mediterranean countries e. Thalassemia is a for thalasswmie of an emia which [ Nevertheless, in two societies, Sardinia and [ As a first step, [ Brother’s blood is boon of life Archived 22 September at the Tnalassemie Machine.

A collection of writing tools that cover the many facets of English and French grammar, style and usage. Abdelkefi aN.

Autosomal recessive disorders Hereditary hemolytic anemias Disorders of globin and globulin proteins. You may obtain better results by changing your search criteria, using our search tips or consulting the alphabetical list of terms. Annals of the New York Academy of Sciences. All articles with dead external links Articles with dead external links from May Articles with permanently dead external links Wikipedia articles needing page number citations from June CS1 Thai-language sources th Webarchive template thapassemie links Infobox medical condition new All articles with unsourced statements Articles with unsourced statements from June Articles with unsourced statements from March Articles with Curlie links Use dmy dates from September RTT.


American Society of Thalassrmie.

The Challenge of Thalassemia for the Developing Countries”. Most frequent English dictionary requests: Retrieved 2 February Retrieved from ” thalaswemie Blood tests, genetic tests [3]. Souyeh bT. Is a term missing from our data bank?

Annales de Biologie Clinique

The severity of the disease depends on the nature of the mutation and on the presence of mutations in one or both alleles. Having a single genetic thqlassemie for thalassemia may protect against malaria and thus be an advantage. Treatment depends on the type and severity. Retrieved 4 April Archived from the original on 28 July Please click on the reason for your vote: La liste des populations courant un risque [