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AI Summary & Key Takeaways
AI Insight⚡ TL;DR(Too Long; Didn't Read)
Wedescribe a child diagnosed with CGD and the p67phox mutation presenting with Serratia marcescens arthritis without osteomyelitis in the newborn period.
📌 3 Key Takeaways
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Objective & Hypothesis:Chronic granulomatous disease (CGD) is a heterogenous genetic primary immune deficiency disorder, characterized by lifethreatening infections and granulomas secondary to increased inflammatory responses.
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Key Findings & Data:Most infections involve the lungs, skin, lymph nodes, and liver.
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Conclusion & Impact:Wedescribe a child diagnosed with CGD and the p67phox mutation presenting with Serratia marcescens arthritis without osteomyelitis in the newborn period.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters
Özet
Chronic granulomatous disease (CGD) is a heterogenous genetic primary immune deficiency disorder, characterized by lifethreatening infections and granulomas secondary to increased inflammatory responses. Most infections involve the lungs, skin, lymph nodes, and liver. Wedescribe a child diagnosed with CGD and the p67phox mutation presenting with Serratia marcescens arthritis without osteomyelitis in the newborn period.
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Cite This Article
CANSEVER, M., KIRÇIL, N., KÖKER, M. Y., PATIROĞLU, T. (2018). Chronic Granulomatous Disease in a Boy Who Presented With Dactilitis Caused by Serratia Marcescens, Mimicking Rheumatic Monoarthritis in the Newborn Period: A Case Presentation. Erciyes Medical Journal, Cilt: 40 - Sayı: 2, 95–98. https://ajindex.com/articles/196104