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Journals / Journal of Clinical and Analytical Medicine / 2011 / Cilt: 2 - Sayı: 1

Association of Diastematomyelia and Klippel-Feil Syndrome: a case report

Diastematomyeli ve Klippel-Feil sendromu birlikteliği: bir olgu sunumu

Ece ÜNLÜ
Ebru UMAY
Recep GAYIR
Şehmuz DEMİR
Aytül ÇAKCI
Pages
40–42
Publication Date
2022-10-18
DOI
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AI Summary & Key Takeaways

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

These anomalies are rarely presentation with together.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Diastematomyelia is an uncommon form of spinal dysraphism that results in the division of the spinal cord into two hemicords with bone, cartilaginous, or fibrous septum.
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Key Findings & Data:Klippel-Feil Syndrome, a congenital skeletal anomalia is characterized by inadequed segmentation of two or more cervical spine.
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Conclusion & Impact:These anomalies are rarely presentation with together.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Diastematomyelia is an uncommon form of spinal dysraphism that results in the division of the spinal cord into two hemicords with bone, cartilaginous, or fibrous septum. Klippel-Feil Syndrome, a congenital skeletal anomalia is characterized by inadequed segmentation of two or more cervical spine. These anomalies are rarely presentation with together.

Özet

Diastematomyeli; kemik, kıkırdak veya fibröz septum ile spinal kanalın 2 parçaya ayrılması ile sonuçlanan, nadir bir konjenital spinal disrafizm formudur. Klippel-Feil sendromu, iki veya daha fazla vertebranın segmentasyon yetersizliği ile karakterize konjenital bir iskelet anomalisidir. Bu anomalilerin birlikte görülmesi nadirdir.

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Cite This Article

ÜNLÜ, E., UMAY, E., GAYIR, R., DEMİR, Ş., ÇAKCI, A. (2022). Association of Diastematomyelia and Klippel-Feil Syndrome: a case report. Journal of Clinical and Analytical Medicine, Cilt: 2 - Sayı: 1, 40–42. https://ajindex.com/articles/561557

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References (8)

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