Nystagmus in Down Syndrome - a Retrospective Notes Review.

Q3 Medicine British and Irish Orthoptic Journal Pub Date : 2022-06-21 eCollection Date: 2022-01-01 DOI:10.22599/bioj.256
Dilys Oladiwura, Yusrah Shweikh, Clare Roberts, Maria Theodorou
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引用次数: 1

Abstract

Introduction: Nystagmus has been reported in up to 30% of people with Down Syndrome (DS), and yet is still not well understood. Our study aims to characterise the clinical features of patients with DS and nystagmus.

Methods: A retrospective medical-records review was conducted of all patients with a diagnosis of DS and nystagmus seen at Moorfields Eye Hospital over a ten-year period.

Results: Fifty-one subjects were identified, with complete data in 48. The mean age at presentation was 5.1 years (range 0-26 years). The mean binocular LogMAR visual acuity was 0.55(95%CI 0.53-0.57), mean refractive error was -1.8 Dioptre Sphere, DS (95% CI - 5.251.63) with -1.2 Dioptre Cylinder, DC (95% CI - 1.6-0.7). Ocular misalignment was found in 50% of patients. A diagnosis of Fusion Maldevelopment Nystagmus Syndrome (FMNS) was made in 6.3%, Infantile Nystagmus Syndrome (INS) in 8.4% and ABducting nystagmus/Inter-Nuclear Ophthalmoplegia (INO) in 2.1%. The descriptive term 'Manifest Horizontal Nystagmus'(MNH) was used in the majority, highlighting the difficulties in clinically differentiating the subtypes of nystagmus in DS. Eleven patients had associated cataract. Additional diagnoses unrelated to DS were made in 10.4%.

Conclusions: The most frequent type of nystagmus in our cohort was 'presumed' INS. This study highlights the importance of differentiating between FMNS and INS (with a latent component), so that further investigations can be performed as appropriate. Almost 25% had associated cataract, and a further 10% other diagnoses un-associated to DS. Despite INS being known to be associated with DS, further investigations may be required in a small subset with true INS after careful clinical assessment and use of eye movement recordings (where available).

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唐氏综合症的眼球震颤-回顾笔记回顾。
导读:据报道,高达30%的唐氏综合征(DS)患者患有眼球震颤,但仍未得到很好的理解。我们的研究旨在描述退行性椎体滑移和眼球震颤患者的临床特征。方法:回顾性分析Moorfields眼科医院10年来诊断为退行性椎体滑移和眼球震颤的所有患者的医疗记录。结果:共纳入51例受试者,其中48例资料完整。平均发病年龄为5.1岁(范围0-26岁)。双眼平均LogMAR视力为0.55(95%CI 0.53-0.57),平均屈光误差为-1.8 Dioptre Sphere, DS (95%CI - 5.251.63)和-1.2 Dioptre Cylinder, DC (95%CI - 1.6-0.7)。50%的患者出现眼部错位。6.3%诊断为融合性发育不良眼震综合征(FMNS), 8.4%诊断为婴儿眼震综合征(INS), 2.1%诊断为外展性眼震/核间性眼麻痹(INO)。“明显水平眼震”(Manifest Horizontal Nystagmus, MNH)一词被广泛使用,突出了临床上区分退行性椎体滑移患者眼震亚型的困难。11例患者合并白内障。与退行性椎体滑移无关的附加诊断占10.4%。结论:我们的队列中最常见的眼球震颤类型为“推定”INS。本研究强调了区分FMNS和INS(有潜在成分)的重要性,因此可以酌情进行进一步的研究。近25%的患者伴有白内障,另有10%的患者的其他诊断与退行性椎体滑移无关。尽管已知INS与退行性痴呆有关,但在仔细的临床评估和使用眼动记录(如有)后,可能需要对一小部分真正INS患者进行进一步的调查。
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来源期刊
British and Irish Orthoptic Journal
British and Irish Orthoptic Journal Health Professions-Optometry
CiteScore
1.50
自引率
0.00%
发文量
13
审稿时长
18 weeks
期刊最新文献
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