Journals / Mustafa Kemal Üniversitesi Tıp Dergisi / 2012 / Cilt: 3 - Sayı: 09

Retrospective analysis of Neural Tube Defect Patients

NÖRAL TÜP DEFEKTLİ HASTALARA RETROSPEKTİF BAKIŞ

Pages
22–28
Publication Date
2015-03-03
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Our study ismulticentric and clinic profiles, therapotic approaches and prognosis of patients with NTD are searched with review of the literature.

📌 3 Key Takeaways

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Objective & Hypothesis:Neural tube defects(NTD) are congenital diseases of almost 1/1000 frequency and occurs with the disclosure of neural tube during the 4th week of embriogenesis.
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Key Findings & Data:Our study ismulticentric and clinic profiles, therapotic approaches and prognosis of patients with NTD are searched with review of the literature.Neural tube defects(NTD) are congenital diseases of almost 1/1000 frequency and occurs with the disclosure of neural tube during the 4th week of embriogenesis.
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Conclusion & Impact:Our study ismulticentric and clinic profiles, therapotic approaches and prognosis of patients with NTD are searched with review of the literature.
🔬Design:Review & Systematic Survey
📍Scope:Comprehensive Sample
⚙️Variables:Nöral tüp defekti · Meningomyelosel · Hidrosefali

Abstract

Neural tube defects(NTD) are congenital diseases of almost 1/1000 frequency and occurs with the disclosure of neural tube during the 4th week of embriogenesis. It may develop from servical to sacral localization and cause neurologic disfunctions with different severities.The etiology is not clear ; genetic and environmental conditions can be accused. Our study ismulticentric and clinic profiles, therapotic approaches and prognosis of patients with NTD are searched with review of the literature.Neural tube defects(NTD) are congenital diseases of almost 1/1000 frequency and occurs with the disclosure of neural tube during the 4th week of embriogenesis. It may develop from servical to sacral localization and cause neurologic disfunctions with different severities.The etiology is not clear ; genetic and environmental conditions can be accused. Our study ismulticentric and clinic profiles, therapotic approaches and prognosis of patients with NTD are searched with review of the literature.

Özet

Nöral tüp defektleri (NTD), yaklaşık 1/1000 sıklığında gözlenen konjenital bir hastalıktır ve embriyogenezisin ilk 4 haftası sırasında nöral tüpün kapanma defekti sonucu oluşur. Servikal bölgeden sakral bölgeye kadar her noktada gelişebilir. Lezyonun seviyesine bağlı olarak çeşitli derecelerde nörolojik disfonksiyonlara sebep olabilir. Etyoloji değişkendir, genetik ve çevresel faktörler suçlanabilir. Bizim bu çalışmamızda incelediğimiz hastalar birden çok merkezden temin edilmiştir ve NTD tanısıyla takip edilen ve doğan hastaların klinik profilleri, tedavi yaklaşımları ve takipleri yeniden araştırılarak literatür ışığında tartışılmıştır.

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Cite This Article

Altaş, M., Aras, M., Altaş, Z., Aras, Z., Serarslan, Y., Yılmaz, N. (2015). Retrospective analysis of Neural Tube Defect Patients. Mustafa Kemal Üniversitesi Tıp Dergisi, Cilt: 3 - Sayı: 09, 22–28. https://ajindex.com/articles/692972

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