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Journals / MN Oftalmoloji / 2009 / Cilt: 16 - Sayı: 4

Retinal astrocytic hamartoma in tuberosclerosis

Tuberosklerozlu olguda retinal astrositik hamartom

Ayşe Ebru BAHADIR
Tahir Kansu BOZKURT
Banu Torun ACAR
Mehmet Şahin SEVİM
Suphi ACAR
Pages
296–299
DOI
—
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AI Summary & Key Takeaways

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

In this study we report retinal astrocytic hamartoma and other systemic finding of a 7 year old child who had a diagnosis of TS.

📌 3 Key Takeaways

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Objective & Hypothesis:Tuberosclerosis (TS) is a neurocutaneous hereditary syndrome characterised by multisystem involvement.
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Key Findings & Data:Retinal astrocytic hamartoma is the classical finding in patients with ocular manifestations.
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Conclusion & Impact:In this study we report retinal astrocytic hamartoma and other systemic finding of a 7 year old child who had a diagnosis of TS.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Tuberosclerosis (TS) is a neurocutaneous hereditary syndrome characterised by multisystem involvement. Retinal astrocytic hamartoma is the classical finding in patients with ocular manifestations. In this study we report retinal astrocytic hamartoma and other systemic finding of a 7 year old child who had a diagnosis of TS.

Özet

Tuberoskleroz (TS), multisistem organ tutulumu ile karakterize, herediter geçişli nörokutanöz bir sendromdur. Oküler tutulumu olan olgularda retinal astrositik hamartom TS’nin klasik göz bulgusudur. Bu çalışmada semptomu olmayan daha önce TS tanısı almış 7 yaşındaki çocuk hastada saptanan retinal astrositik hamartom ve eşlik eden diğer sistemik bulgular bildirilmiştir.

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Cite This Article

BAHADIR, A. E., BOZKURT, T. K., ACAR, B. T., SEVİM, M. Ş., ACAR, S. (2009). Retinal astrocytic hamartoma in tuberosclerosis. MN Oftalmoloji, Cilt: 16 - Sayı: 4, 296–299. https://ajindex.com/articles/296822

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References (1)

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