Addressing kyphoscoliosis in Gaucher’s disease: a multidisciplinary approach to a rare case
Jianwei Guo, Li Zhang, Changlin Lv, Tianyu Bai, Jiale Shao, Yongming Xi · 2026
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Description
BackgroundGaucher’s disease (GD) is a rare autosomal recessive disorder caused by mutations in the GBA gene, leading to glucocerebrosidase deficiency and the accumulation of glucosyl ceramide in the bone marrow, which can result in skeletal complications such as scoliosis and kyphosis. Surgical interventions for orthopedic manifestations in GD are challenging and have been rarely reported.Study designA clinical retrospective study.
Catalog record
| CREATOR | Jianwei Guo, Li Zhang, Changlin Lv, Tianyu Bai, Jiale Shao, Yongming Xi |
|---|---|
| YEAR | 2026 |
| COLLECTION | PAPERS |
| FORMAT | TXT |
| FILE SIZE | 21 KB |
| VERSION | 1.0 |
| LICENSE | CC BY 4.0 |
| RIGHTS | CC BY |
| SOURCE | Europe PMC |