卢斯卡-卢米什综合征:一个病例报告
Bogumiła Wójcik-Niklewska1,2, Erita Filipek1
1Department of Pediatric Ophtalmology, Faculty of Medical Sciences in Katowice, Medical University of Silesia in Katowice, Katowice 40-514, Silesia, Poland.
World journal of clinical cases
|June 27, 2025
概括
卢斯坎-卢米什综合征 (LLS) 是一种罕见的遗传疾病. 这一案例突显了LLS儿童的眼部异常,包括视野缺陷和改变的电生理反应,强调了定期进行眼科检查的必要性.
科学领域:
- 眼科医生 眼科 眼科
- 遗传学 遗传学 是一个
- 神经发育障碍 神经发育障碍
背景情况:
- 卢斯坎-卢米什综合征 (LLS) 是一种罕见的遗传疾病,其特征是神经发育问题和偶尔的眼部异常.
- 这篇论文详细介绍了一例儿科遗传确诊LLS的眼科发现.
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