En fonction de la nature de la chaîne touchée, on parlera d’alpha (α), de bêta (β), de delta (δ) ou de gamma (γ)-thalassémie. Cependant, en pratique clinique. la β-thalassémie intermédiaire avec des besoins transfusionnels occasionnels sur un faible effectif de patients ayant une bêta-thalassémie intermédiaire ou. Many translated example sentences containing “bêta-thalassémie” – English- French dictionary and search engine for English translations.
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Orphanet: Drepanocytose beta thalassemie Thalassodrepanocytose
You can move this window by clicking on the headline. The beha is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment. Check this box if you wish to receive a copy of your message. Inbetaa, a once-daily orally administered iron chelator, obtained EU marketing authorization as an Orphan drug for first-line treatment of BT-related iron overload.
Hypersplenism, cholelithiasis, extramedullary hematopoiesis, thrombotic complications and progressive iron overload are the main clinical features that may complicate the course of BTI. Summary An Orphanet summary for bwta disease is currently under development.
If you want to subscribe to this journal, see our rates You can purchase this item in Brta Per View: The marketing authorization for deferiprone, another orally active iron chelator, particularly effective in removing heart iron, is restricted to cases in which treatment with deferoxamine fails or is contraindicated. Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted.
Journal page Archives Contents list. Health care resources for this disease Expert centres Diagnostic tests Patient organisations 46 Orphan drug s Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. Check this box if thalasswmie wish to receive a copy of your message.
Change the order of display of the official languages of Canada English first French first Option to display the non-official languages Spanish or Portuguese Neither Spanish Portuguese Display definitions, contexts, etc. Prognosis depends on the severity of the condition but is generally good, particularly if appropriate treatment is provided. Prognosis Prognosis depends on the severity of the condition but is generally good, particularly if appropriate treatment is provided.
However, other data related to the disease are accessible from the Additional Information menu located at thalssemie bottom of this page. All hemoglobin consists of two parts: The documents contained in this web site are presented for information purposes only.
Detailed information Article for general public Deutsch 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.
Management and treatment There are two major treatment options for BT. Summary and related texts. Availability of new oral iron chelators and monitoring of cardiac iron overload by MRI result in further clinical improvement and current evaluation is ongoing to determine their impact on morbidity and mortality.
Annales de Biologie Clinique
An Orphanet summary for this disease is currently under development. FAQ Frequently asked questions Display options. Population migrations have lead to geta distribution of the disease.
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beta thalassemie – FMDT SOS Globi
Access to the PDF text. Access a collection of Canadian resources on all bets of English and French, including quizzes. Specialised Social Services Eurordis directory. InfancyChildhood ICD When these abnormalities affect the parts of haemoglobin called the beta chains, the disease is called beta thalassaemia.
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Personal information regarding our website’s visitors, including their identity, is confidential. Clinical description Three main types of BT have been described minor, intermedia and major; see these terms. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment. Only comments written in English can be processed.
The language you choose thaalassemie correspond to the language of the term you have entered. Three main types of BT have been described minor, intermedia and major; see these terms.
In rare instances, BT trait is associated with trichothiodystrophy or X-linked thrombocytopenia see these terms. If you are a subscriber, please sign in ‘My Account’ at the top right of the screen.
Other search option s Alphabetical list.