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

Child S Nervous System · Ocak 2019

Özet
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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YÖKSİS Kayıtları
Cauda equina syndrome in a patient diagnosed with type 1 Gaucher disease: a rare case
CHILDS NERVOUS SYSTEM · 2019 SSCI
Prof. Dr. ENDER KÖKTEKİR →
Cauda equina syndrome in a patient diagnosed with type 1 Gaucher disease: a rare case
CHILDS NERVOUS SYSTEM · 2019 SCI-Expanded
Prof. Dr. ENDER KÖKTEKİR →
Cauda equina syndrome in a patient diagnosed with type 1 Gaucher disease: a rare case
CHILDS NERVOUS SYSTEM · 2019 SCI-Expanded
Doç. Dr. MERT ŞAHİNOĞLU →
YÖKSİS Kayıtları — ISSN Eşleşmesi
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Cauda equina syndrome in a patient diagnosed with type 1 Gaucher disease: a rare case
2019 ISSN: 0256-7040 SCI-Expanded
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Cauda equina syndrome in a patient diagnosed with type 1 Gaucher disease: a rare case
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Prof. Dr. ENDER KÖKTEKİR →
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Makale Bilgileri

Toplam Atıf 0 atıf · Scopus
ISSN02567040
Yayın TarihiOcak 2019
Cilt / Sayfa35 · 191-194

Kurumlar

Selçuk Üniversitesi
Selçuklu Turkey
Serik State Hospital
Antakya Turkey

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Bu makaleye, sistemimizdeki Scopus veritabanında bulunan 0 makale atıf yapmıştır.

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Scimago Dergi (ISSN Eşleşmesi)
Child's Nervous System
Q2
SJR Skoru0,452
H-Index106
YayıncıSpringer Science and Business Media Deutschland GmbH
ÜlkeGermany
Pediatrics, Perinatology and Child Health (Q2)
Medicine (miscellaneous) (Q3)
Neurology (clinical) (Q3)
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