Cauda equina syndrome in a patient diagnosed with type 1 Gaucher disease: a rare case
Yükleniyor...
Dosyalar
Tarih
2019
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
SPRINGER
Erişim Hakkı
info:eu-repo/semantics/openAccess
Özet
BackgroundGaucher 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.
Açıklama
Anahtar Kelimeler
Gaucher, Cauda equina, Sacral mass
Kaynak
CHILDS NERVOUS SYSTEM
WoS Q Değeri
Q3
Scopus Q Değeri
Q2
Cilt
35
Sayı
1
Künye
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.
