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夏尔沃-萨格奈常染色体隐性痉挛性共济失调中视网膜神经纤维层增厚且无髓鞘增多

Thickened Retinal Nerve Fiber Layer Without Hypermyelination in Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay.

作者信息

Suarez Mallory K, Martin Timothy J, Ong Sally S

机构信息

Department of Ophthalmology, Wake Forest School of Medicine, Winston-Salem, NC, USA.

出版信息

J Vitreoretin Dis. 2024 May 6;8(4):466-470. doi: 10.1177/24741264241251582. eCollection 2024 Jul-Aug.

Abstract

To report the retinal findings in a patient with autosomal recessive spastic ataxia of Charlevoix-Saguenay. A case was evaluated. A 16-year-old male patient with a known diagnosis of autosomal recessive spastic ataxia of Charlevoix-Saguenay was referred for evaluation of retinal hypermyelination given its frequent association with the condition. The patient was asymptomatic with a best-corrected visual acuity of 20/20. Optical coherence tomography of the peripapillary retinal nerve fiber layer (RNFL) showed bilateral thickening in each eye (average thicknesses: 180 µm, right eye; 177 µm, left eye). An examination showed no myelinization of the RNFL. Most studies to date describe RNFL thickening secondary to hypermyelination as a characteristic finding in autosomal recessive spastic ataxia of Charlevoix-Saguenay. This case provides evidence that this thickening may be a result of hypertrophy rather than hypermyelination. Further investigation is needed to define the pathophysiologic cause of RNFL thickening in autosomal recessive spastic ataxia of Charlevoix-Saguenay.

摘要

报告一名患有常染色体隐性遗传性夏勒沃魁 - 萨格奈痉挛性共济失调患者的视网膜检查结果。对一例病例进行了评估。一名已知诊断为常染色体隐性遗传性夏勒沃魁 - 萨格奈痉挛性共济失调的16岁男性患者因视网膜高髓鞘化与该疾病频繁相关而被转诊进行评估。该患者无症状,最佳矫正视力为20/20。视乳头周围视网膜神经纤维层(RNFL)的光学相干断层扫描显示每只眼睛均有双侧增厚(平均厚度:右眼180 µm;左眼177 µm)。检查显示RNFL无髓鞘化。迄今为止,大多数研究将继发于高髓鞘化的RNFL增厚描述为常染色体隐性遗传性夏勒沃魁 - 萨格奈痉挛性共济失调的特征性表现。该病例提供了证据表明这种增厚可能是肥大而非高髓鞘化的结果。需要进一步研究以确定常染色体隐性遗传性夏勒沃魁 - 萨格奈痉挛性共济失调中RNFL增厚的病理生理原因。

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