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Abstracts tagged "Lysosomal Storage Disorder"

  • Abstract Number: 904 • 2019 ACR/ARP Annual Meeting

    Bone Manifestations in Gaucher Disease: A Monocentric Study of 128 Patients

    Yann Nguyen1, Jérôme Stirnemann 2, Monia Bengherbia 1, Karima Yousfi 1, Dalil Hamroun 3, Wassim Allaham 4, Bruno Fantin 4 and Nadia Belmatoug 1, 1Centre de reference des maladies lysosomales, Hôpital Beaujon, AP-HP, Clichy, France, 2Hôpitaux Universitaires de Genève, Genève, Switzerland, 3CHRU de Montpellier, Montpellier, France, 4Hôpital Beaujon, AP-HP, Clichy, France

    Background/Purpose: Gaucher disease (GD) is a rare lysosomal storage disorder caused by mutations in the glucocerebrosidase gene, leading to defective lysosomal acid β-glucosidase. Its incidence…
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