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Journals / Kartal Eğitim ve Araştırma Hastanesi Tıp Dergisi / 2015 / Cilt: 26 - Sayı: 3

Two Cases of Spina Bifida and Renal Anomaly with Differing Findings

Farklı Bulguları Olan Spina Bifida ve Renal Anomalili İki Olgu Sunumu

Meral KARAOĞUZ YİRMİBEŞ
Ali KARAMAN
Bilge GEÇKİNLİ
Halil İbrahim ATASOY
Hatip AYDIN
M. Arzu YOLDAŞ
Erkan YEŞİLLER
Esra TUĞ
Pages
272–276
Publication Date
2022-10-17
DOI
—
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AI Summary & Key Takeaways

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

The first patient presented with unilateral renal agenesis, spina bifida, hydrocephalus, and plegia.The second presented with spina bifida, hydrocephalus, plegia, polydactyly, anal atresia, and unilateral renal hypoplasia.Though both patients had the same neural tube defect, findings differed.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Neural tube defects arise from failure of embryonic development in 4th 6th weeks.
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Key Findings & Data:The cases of twomale patients aged 9 and 12 years with spina bifida and renalanomaly are described.
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Conclusion & Impact:The first patient presented with unilateral renal agenesis, spina bifida, hydrocephalus, and plegia.The second presented with spina bifida, hydrocephalus, plegia, polydactyly, anal atresia, and unilateral renal hypoplasia.Though both patients had the same neural tube defect, findings differed.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Neural tube defects arise from failure of embryonic development in 4th 6th weeks. Defects of the cranial region (anenceph- aly) and lower spine (open spina bifida, myelomeningocele)are the most common neural tube defects. The cases of twomale patients aged 9 and 12 years with spina bifida and renalanomaly are described. The first patient presented with unilateral renal agenesis, spina bifida, hydrocephalus, and plegia.The second presented with spina bifida, hydrocephalus, plegia, polydactyly, anal atresia, and unilateral renal hypoplasia.Though both patients had the same neural tube defect, findings differed.

Özet

Nöral tüp defekti embriyonel gelişimin 4 ve 6. haftalar arasın- da tamamlanması gereken nöral tüpün kapanma bozukluk- larından kaynaklanır. Nöral tüp defektinde en sık etkilenmekranial kısım (anensefali) ve alt vertebra seviyesinde (açıkspina bifida, meningomyelosel) görülür. Spina bifida ve renalanomalili dokuz ve 12 yaşınlarında iki erkek olgu değerlendi- rildi. İlk olguda spina bifida, hidrosefali, pleji, tek taraflı böb- rek agenezisi, ikinci olguda spina bifida, hidrosefali, pleji, po- lidaktili, anal atrezi, böbrek hipoplazisi mevcuttu. Aynı tanıyasahip olmalarına rağmen iki olgunun bulguları birbirlerindenoldukça farklıydı.

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Cite This Article

YİRMİBEŞ, M. K., KARAMAN, A., GEÇKİNLİ, B., ATASOY, H. İ., AYDIN, H., YOLDAŞ, M. A., YEŞİLLER, E., TUĞ, E. (2022). Two Cases of Spina Bifida and Renal Anomaly with Differing Findings. Kartal Eğitim ve Araştırma Hastanesi Tıp Dergisi, Cilt: 26 - Sayı: 3, 272–276. https://ajindex.com/articles/571314

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