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Journals / Türk Osteoporoz Dergisi / 2020 / Cilt: 26 - Sayı: 2

Osteomalacia due to Vitamin D Deficiency: A Case Report

D Vitamini Eksikliğine Bağlı Osteomalazi: Olgu Sunumu

Banu ORDAHAN
Kaan USLU
Hatice UĞURLU
Pages
143–145
Publication Date
2022-11-06
DOI
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AI Summary & Key Takeaways

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

Patient was treated with vitamin D.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Osteomalacia is a metabolic bone disease characterized by demineralization of the newly formed osteoid in adults.
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Key Findings & Data:Here,we present the case of 18 year old female patient who presented to our hospital with complaints of low back pain.
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Conclusion & Impact:Patient was treated with vitamin D.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Osteomalacia is a metabolic bone disease characterized by demineralization of the newly formed osteoid in adults. Vitamin D deficiency due to insufficient vitamin D intake, inadequate exposure to sunlight, and malabsorption of vitamin D are the most widespread cause of osteomalacia. Here,we present the case of 18 year old female patient who presented to our hospital with complaints of low back pain. Sacral bone pseudofracture was detected by magnetic resonance imaging due to osteomalacia. Patient was treated with vitamin D.

Özet

Osteomalazi, yetişkinlerde yeni oluşan osteoidin mineralleşmesinde azalma ile karakterize metabolik bir kemik hastalığıdır. Yetersiz D vitamini alımı, güneş ışığına yetersiz maruz kalma ve D vitamini malabsorpsiyonu nedeniyle D vitamini eksikliği, osteomalazinin en sık nedenidir. Bu yazıda, bel ağrısı şikayeti ile hastaneye başvuran 18 yaşında kadın hastayı sunduk. Osteomalazi nedeniyle manyetik rezonans görüntüleme ile sakral kemik psödofraktürü saptandı. Hasta D vitamini ile tedavi edildi.

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Cite This Article

ORDAHAN, B., USLU, K., UĞURLU, H. (2022). Osteomalacia due to Vitamin D Deficiency: A Case Report. Türk Osteoporoz Dergisi, Cilt: 26 - Sayı: 2, 143–145. https://ajindex.com/articles/639642

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