Inflammatory arthritis complicating galactosialidosis: a case report

BACKGROUND: Galactosialidosis (GS) is a rare inherited lysosomal storage disorder (LSD) which is characterized by a defect in the lysosomal glycoprotein catabolism. We report, for the first time, the case of a child affected by GS presenting with recurrent episodes of extensive joint inflammation in...

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Detalles Bibliográficos
Autores principales: Verkuil, F., Bosch, A. M., Struijs, P. A. A., Hemke, R., van den Berg, J. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8504000/
https://www.ncbi.nlm.nih.gov/pubmed/34629108
http://dx.doi.org/10.1186/s41927-021-00208-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8504000/
https://www.ncbi.nlm.nih.gov/pubmed/34629108
http://dx.doi.org/10.1186/s41927-021-00208-0

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