Journals / Haseki Tıp Bülteni / 2001 / Cilt: 39 - Sayı: 1

Gaucher disease

Günümüzün tedavi edilebilen bir lipid depo hastalığı: Gaucher hastalığı

Pages
69–71
DOI
—
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AI Summary & Key Takeaways

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

Even it is rarely observed in childhood, we have presented this case because ofability of recovery with therapy in last years.

📌 3 Key Takeaways

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Objective & Hypothesis:Gaucher disease is the most common lysosomal storage disorder.
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Key Findings & Data:With physical and laboratory investigations of a 9 month agedfemale, abdominal distantlon, weight loss and respiratory distress symptoms, we have diagnosed the infantil type Gaucher's disease.
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Conclusion & Impact:Even it is rarely observed in childhood, we have presented this case because ofability of recovery with therapy in last years.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Gaucher hastalığı · Süt çocuğu · yenidoğan

Abstract

Gaucher disease is the most common lysosomal storage disorder. With physical and laboratory investigations of a 9 month agedfemale, abdominal distantlon, weight loss and respiratory distress symptoms, we have diagnosed the infantil type Gaucher's disease. Even it is rarely observed in childhood, we have presented this case because ofability of recovery with therapy in last years.

Özet

Gaucher hastalığı en sık görülen bir lizozomal depo hastalığıdır. Karın şişliği, kilo alamama, solunum sıkıntısı ile başvuran 9 aylık bir kız hastada yapılan tetkikler sonucunda infantil tip Gaucher hastalığı tanısı konuldu. Çocukluk çağında ender görülmesine rağmen günümüzde tedavisinin mümkün olması nedeniyle bu olguyu sunmayı uygun bulduk.

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Cite This Article

URGANCI, N., ÖZÇELİK, G., EVRÜKE, M., NUHOĞLU, A. (2001). Gaucher disease. Haseki Tıp Bülteni, Cilt: 39 - Sayı: 1, 69–71. https://ajindex.com/articles/268129