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Journals / Güncel Retina Dergisi / 2022 / Cilt: 6 - Sayı: 2

Optic Neuropathies in Neurodegenerative Disorders of Childhood

Çocukluk Çağı Nörodejeneratif Bozukluklarında Optik Nöropatiler

Berker BAKBAK
Pages
109–112
Publication Date
2022-10-17
DOI
—
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AI Summary & Key Takeaways

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

In this review, optic neuropathies in neurodegenerative disorders of childhood are discussed.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:The hereditary optic neuropathies comprise a group of hereditable disorders accompanied with optic nerve dysfunctions.
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Key Findings & Data:Due to clinical variability, diagnose and classification of the disease is difficult.
💡
Conclusion & Impact:In this review, optic neuropathies in neurodegenerative disorders of childhood are discussed.
🔬Design:Review & Systematic Survey
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

The hereditary optic neuropathies comprise a group of hereditable disorders accompanied with optic nerve dysfunctions. Due to clinical variability, diagnose and classification of the disease is difficult. In some hereditary optic neuropathies, optic nerve dysfunction is the only sign of the disease, whereas the others include various neurologic and systemic abnormalities. In this review, optic neuropathies in neurodegenerative disorders of childhood are discussed.

Özet

Herediter optik nöropatiler, optik sinir fonksiyonlarında azalma ile seyreden genetik geçişli bir grup hastalığı içerir. Bu hastalık grupları, klinik olarak değişkenlik gösterdiğinden tanı ve sınıflama kolay olmamaktadır. Bazı herediter optik nöropatilerde, optik sinirde fonksiyon kaybı, hastalığın tek bulgusudur. Diğerlerinde çeşitli nörolojik ve sistemik anormallikler eşlik eder. Bu derlemede, çocukluk çağında nörodejeneratif bozukluklarında optik nöropatiler ele alınmıştır.

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Cite This Article

BAKBAK, B. (2022). Optic Neuropathies in Neurodegenerative Disorders of Childhood. Güncel Retina Dergisi, Cilt: 6 - Sayı: 2, 109–112. https://ajindex.com/articles/528147

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