The French Gaucher’s disease registry: clinical characteristics, complications and treatment of 562 patients

The French Gaucher’s disease registry: clinical characteristics, complications and treatment of 562 patients

<p>Abstract</p> <p>Background</p> <p>Clinical features, complications and treatments of Gaucher’s disease (GD), a rare autosomal–recessive disorder due to a confirmed lysosomal enzyme (glucocerebrosidase) deficiency, are described.</p> <p>Methods</p> &...

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Bibliographic Details
Main Authors: Stirnemann Jérôme, Vigan Marie, Hamroun Dalil, Heraoui Djazia, Rossi-Semerano Linda, Berger Marc G, Rose Christian, Camou Fabrice, de Roux-Serratrice Christine, Grosbois Bernard, Kaminsky Pierre, Robert Alain, Caillaud Catherine, Froissart Roselyne, Levade Thierry, Masseau Agathe, Mignot Cyril, Sedel Frédéric, Dobbelaere Dries, Vanier Marie T, Valayanopoulos Vassili, Fain Olivier, Fantin Bruno, de Villemeur Thierry, Mentré France, Belmatoug Nadia
Format: Article
Language:English
Published: BMC 2012-10-01
Series:Orphanet Journal of Rare Diseases
Subjects:
French Gaucher’s Disease Registry
Bone events
Enzyme-replacement therapy
Online Access:http://www.ojrd.com/content/7/1/77

Internet

http://www.ojrd.com/content/7/1/77

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