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AI Summary & Key Takeaways
AI Insight⚡ TL;DR(Too Long; Didn't Read)
In our report, a case of retinitis pigmentosa with adult type Gaucher's disease is presented.
📌 3 Key Takeaways
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Objective & Hypothesis:Gaucher's disease is a rare, chronically progressive, hereditary lipid storage disorder.
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Key Findings & Data:Retinitis pigmentosa is a retinal dystrophia and there is no evidence in the literature of its link with Gaucher's disease.
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Conclusion & Impact:In our report, a case of retinitis pigmentosa with adult type Gaucher's disease is presented.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters
Abstract
Gaucher's disease is a rare, chronically progressive, hereditary lipid storage disorder. Retinitis pigmentosa is a retinal dystrophia and there is no evidence in the literature of its link with Gaucher's disease. In our report, a case of retinitis pigmentosa with adult type Gaucher's disease is presented.
Özet
Gaucher hastalığı nadir görülen, kronik seyirli, ailevi geçiş gösteren bir lipid depo hastalığıdır. Retinitis pigmentosa ise retinal distrofidir. Literatürde Gaucher hastalığı ile beraberliğine rastlanmamıştır. Yazımızda, erişkin tip Gaucher hastalığı ile beraber olan retinis pigmentosa olgusu sunuldu.
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Cite This Article
KAYA, N., KETENCİ, M., KOŞAR, A., ARITÜRK, N., AKPOLAT, İ., ALTINTOP, L., KAHRAMAN, H. (1998). Gaucher' s disease and retinitis pigmentosa: A case report. Turkish Journal of Gastroenterology, Cilt: 9 - Sayı: 4, 377–380. https://ajindex.com/articles/411486