Journals / Güncel Pediatri / 2008 / Cilt: 6 Sayı: 5

Retinitis Pigmentosa in Childhood: A Case Report

Çocukluk Çağında Retinitis Pigmentosa: Bir Olgu Sunumu

Erdal Eren(Uludağ Üniversitesi Tıp Fakültesi Çocuk Sağlığı ve Hastalıkları Anabilim Dalı, Çocuk Endokrinoloji Bilim Dalı, Bursa)
Ufuk Şahin Tığ(Süleyman Demirel Üniversitesi Tıp Fakültesi)
Fadime Kendir(Süleyman Demirel Üniversitesi Tıp Fakültesi)
Ali Ayata(Çocuk Sağlığı ve Hastalıkları Anabilim Dalı , Isparta, Türkiye)
Pages
43–46
Publication Date
2008-12-01
DOI
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AI Summary & Key Takeaways

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

We present apatient with RP and describe diagnosis, treatment and approach to this disease

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Retinitis pigmentosa RP is characterized by progressive loss of vision andaccompanied by many syndromes.
📊
Key Findings & Data:Therefore, early diagnosis is very importantin RP.
💡
Conclusion & Impact:We present apatient with RP and describe diagnosis, treatment and approach to this disease
🔬Design:Makale
📍Scope:Comprehensive Sample
⚙️Variables:Retinitis pigmentoza · çocuk · görme kaybı

Abstract

Retinitis pigmentosa RP is characterized by progressive loss of vision andaccompanied by many syndromes. Therefore, early diagnosis is very importantin RP. Now, definitive treatment of RP is not available. Diagnosis is performedwith good medical history and ophthalmolojical examination. We present apatient with RP and describe diagnosis, treatment and approach to this disease

Özet

Retinitis pigmentoza RP , birçok sendromla birlikte bulunabilen ve ilerleyicigörme kaybıyla seyreden bir hastalıktır. Bu nedenle erken tanısı önemlidir.Halen tedavisi bulunmayan bu hastalığın tanısı, iyi bir anamnez ve oftalmolojikmuayene ile konulabilmektedir. Bu yazıda bir olgu sunularak RP’ye yaklaşım,tanı ve tedavi yolları anlatılmıştır

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Cite This Article

Eren, E., Tığ, U. Ş., Kendir, F., Ayata, A. (2008). Retinitis Pigmentosa in Childhood: A Case Report. Güncel Pediatri, Cilt: 6 Sayı: 5, 43–46. https://ajindex.com/articles/1401181

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