O02: Baseline characteristics of a real-world population with alpha-mannosidosis: Insights from the SPARKLE Registry*
Nicole Muschol,
Nathalie Guffon,
Andrea Ballabeni,
Line Borgwardt,
Allan Lund,
Mercedes Gil-Campos,
Francesca Dona,
Julia Hennermann
Affiliations
Nicole Muschol
European Reference Network for Hereditary Metabolic Disorders; International Center for Lysosomal Disorders, University Medical Center Hamburg-Eppendorf, Hamburg, Germany
Nathalie Guffon
Reference Centre for Inherited Metabolic Diseases, CERLYMM, Hospices Civils de Lyon, Lyon, France
Andrea Ballabeni
Chiesi Farmaceutici S.p.A., Parma, Italy
Line Borgwardt
Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark
Allan Lund
European Reference Network for Hereditary Metabolic Disorders; Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark
Mercedes Gil-Campos
Reina Sofía University Hospital, IMIBIC, University of Cordoba, CIBEROBN, Córdoba, Spain
Francesca Dona
Chiesi Farmaceutici S.p.A., Parma, Italy
Julia Hennermann
European Reference Network for Hereditary Metabolic Disorders; Villa Metabolica, University Medical Center Mainz, Mainz, Germany
