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Journals / Türkiye Çocuk Hastalıkları Dergisi / 2014 / Cilt: 8 - Sayı: 1

A Case with Malignant Osteopetrosis

Malign Osteopetrozisli Bir Olgu

İlknur BODUR
Gonca YILMAZ
M. Melek OĞUZ
Can Demir KARACAN
Pelin ZORLU
Pages
35–38
Publication Date
2022-11-05
DOI
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AI Summary & Key Takeaways

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

In this article we reported a case diagnosed as malign osteopetrosis while investigating the causes of anemia and hepatosplenomegaly

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Osteopetrosis is a hereditary disorder that is caused by a bone resorption defect and characterized with diffuse sclerosis of the bones.
📊
Key Findings & Data:The severe form is detected in infancy because of macrocephaly, hepatosplenomegaly, deafness, blindness, and severe anemia.
💡
Conclusion & Impact:In this article we reported a case diagnosed as malign osteopetrosis while investigating the causes of anemia and hepatosplenomegaly
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:İnfant · Osteopetrozis · Osteosklerozis

Abstract

Osteopetrosis is a hereditary disorder that is caused by a bone resorption defect and characterized with diffuse sclerosis of the bones. The severe form is detected in infancy because of macrocephaly, hepatosplenomegaly, deafness, blindness, and severe anemia. In this article we reported a case diagnosed as malign osteopetrosis while investigating the causes of anemia and hepatosplenomegaly

Özet

Osteopetrozis kemik rezorpsiyon kusuru nedeniyle oluşan yaygın kemik sklerozuyla karekterize kalıtımsal bir hastalıktır. Osteopetrozisin malign formu infantlarda makrosefali, hepatosplenomegali, sağırlık, körlük ve ciddi anemiyle farkedilir. Hepatosplenomegali ve anemi nedeni araştırılırken malign osteopetrosiz tanısı alan hasta sunuldu.

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Cite This Article

BODUR, İ., YILMAZ, G., OĞUZ, M. M., KARACAN, C. D., ZORLU, P. (2022). A Case with Malignant Osteopetrosis. Türkiye Çocuk Hastalıkları Dergisi, Cilt: 8 - Sayı: 1, 35–38. https://ajindex.com/articles/626617

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References (9)

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