Journals / Ondokuz Mayıs Üniversitesi Tıp Dergisi (. Journal of Experimental and Clinical Medicine) / 2001 / Cilt: 18 - Sayı: 2

The case of sirenomelia

Bir sirenomeli olgusu

Pages
131–134
DOI
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AI Summary & Key Takeaways

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

We presented a case at sirenomelia in the non-diabetic mother and discussed the light of literature

📌 3 Key Takeaways

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Objective & Hypothesis:Sirenomelia is rare developmental anomaly that characterized by fusion of the lower limb buds and sacral agenesis.
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Key Findings & Data:Sirenomelia is rare developmental anomaly that characterized by fusion of the lower limb buds and sacral agenesis.
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Conclusion & Impact:We presented a case at sirenomelia in the non-diabetic mother and discussed the light of literature
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Düşük · istemli · Ektromeli

Abstract

Sirenomelia is rare developmental anomaly that characterized by fusion of the lower limb buds and sacral agenesis. We presented a case at sirenomelia in the non-diabetic mother and discussed the light of literature

Özet

Sirenomeli alt ekstremitelerin füzyonu ve sakral agenezis ile karakterize nadir bir gelişimsel anomalidir. Biz, diyabetik olmayan annede sirenomeli olgusunu literatür ışığında tartıştık.

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Cite This Article

YILDIZ, L., KURT, K., AYDIN, O., YALIN, T. (2001). The case of sirenomelia. Ondokuz Mayıs Üniversitesi Tıp Dergisi (. Journal of Experimental and Clinical Medicine), Cilt: 18 - Sayı: 2, 131–134. https://ajindex.com/articles/293366