Cauda equina syndrome in a patient diagnosed with type 1 Gaucher disease: a rare case

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Abstract

Background: Gaucher disease is a rare hereditary glycolipid storage disease. One of the rare complications is neurodeficits due to vertebral involvement. Case presentation: An 18-year-old female patient presented to the outpatient clinic with cauda equina syndrome due to sacral involvement of type 1 GD. Bilateral laminectomy via posterior approach without posterior stabilization was performed. Conclusion: Maximum excision of the mass avoiding destabilization of the spinal column can provide long-term vertebral stability and improvement in neurodeficits.

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Sahinoglu, M., Mutlukan, A., Koktekir, E., & Karabagli, H. (2019). Cauda equina syndrome in a patient diagnosed with type 1 Gaucher disease: a rare case. Child’s Nervous System, 35(1), 191–194. https://doi.org/10.1007/s00381-018-3946-z

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