Sahinoglu, M.Mutlukan, A.Koktekir, E.Karabagli, H.2020-03-262020-03-262019Sahinoglu, 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), 191-194.0256-70401433-0350https://dx.doi.org/10.1007/s00381-018-3946-zhttps://hdl.handle.net/20.500.12395/37555BackgroundGaucher disease is a rare hereditary glycolipid storage disease. One of the rare complications is neurodeficits due to vertebral involvement.Case presentationAn 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.ConclusionMaximum excision of the mass avoiding destabilization of the spinal column can provide long-term vertebral stability and improvement in neurodeficits.en10.1007/s00381-018-3946-zinfo:eu-repo/semantics/openAccessGaucherCauda equinaSacral massArticle35119119430094495Q2WOS:000456311300029Q3