Ocular Findings in Jansen Metaphyseal Chondrodysplasia

IF 3.4 Q2 ENDOCRINOLOGY & METABOLISM JBMR Plus Pub Date : 2024-07-12 DOI:10.1093/jbmrpl/ziae089
Fiona Obiezu, M. T. M. D. Q. Costa, Laryssa A. Huryn, Kristen Pan, K. Almpani, Anisha Ninan, KL Roszko, Lee S Weinstein, R. Gafni, Carlos R Ferreira, Janice Lee, Michael T Collins, Smita Jha
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Abstract

Jansen Metaphyseal Chondrodysplasia (JMC) is an ultra-rare disorder caused by germline heterozygous PTHR1 variants resulting in constitutive activation of parathyroid hormone type 1 receptor (PTHR1) with only 30 patients identified globally. A description of ocular manifestations of the disease is lacking. Six patients with JMC underwent a detailed ophthalmic evaluation, spectral-domain optical coherence tomography (OCT), visual field testing and craniofacial CT scans. Five of six patients had good visual acuity. All patients had widely spaced eyes; 5/6 had downslanted palpebral fissures. One patient had proptosis, and another had bilateral ptosis. Two patients had incomplete closure of the eyelids (lagophthalmos), one had a history of progressive right facial nerve palsy with profuse epiphora while the second had advanced optic nerve atrophy with corresponding retinal nerve fiber layer (RNFL) thinning on OCT and significant bilateral optic canal narrowing on CT scan. Additionally, this patient also had central visual field defects, and abnormal color vision. A third patient had normal visual acuity, subtle temporal pallor of the optic nerve head, normal average RNFL, but decreased temporal RNFL and retinal ganglion cell layer analysis (GCA) on OCT. GCA was decreased in 4/6 patients indicating a subclinical optic nerve atrophic process. None of the patients had glaucoma or high myopia. These data represent the first comprehensive report of ophthalmic findings in JMC. Patients with JMC have significant eye findings associated with optic canal narrowing due to extensive skull base dysplastic bone overgrowth that appear to be more prevalent and pronounced with age. Progressive optic neuropathy from optic canal narrowing may be a feature of JMC and OCT GCA can serve as a useful biomarker for progression in the setting of optic canal narrowing. We suggest that patients with JMC should undergo regular ophthalmic examination including color vision, OCT, visual field testing, orbital and craniofacial imaging.
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詹森骺软骨发育不良症的眼部表现
詹森骺软骨发育不良症(JMC)是一种超罕见的疾病,由种系杂合子PTHR1变异导致甲状旁腺激素1型受体(PTHR1)组成性激活引起,全球仅发现30例患者。目前尚缺乏对该病眼部表现的描述。六名 JMC 患者接受了详细的眼科评估、光谱域光学相干断层扫描(OCT)、视野测试和头面部 CT 扫描。六名患者中有五名视力良好。所有患者的眼距都很宽;5/6 患者的睑裂向下倾斜。一名患者有眼睑下垂,另一名患者有双侧眼睑下垂。两名患者眼睑闭合不全(眼睑下垂),一名患者有进行性右侧面神经麻痹病史,伴有大量眼外窥,另一名患者有晚期视神经萎缩,OCT检查显示视网膜神经纤维层(RNFL)相应变薄,CT扫描显示双侧视神经管明显狭窄。此外,这名患者还伴有中心视野缺损和色觉异常。第三位患者视力正常,视神经头颞侧有轻微苍白,平均 RNFL 正常,但颞侧 RNFL 和视网膜神经节细胞层分析(GCA)在 OCT 上下降。4/6 名患者的 GCA 下降,表明存在亚临床视神经萎缩过程。所有患者均无青光眼或高度近视。这些数据首次全面报告了 JMC 患者的眼科检查结果。JMC患者的眼部病变与广泛的颅底发育不良骨质增生导致的视神经管狭窄有关,随着年龄的增长,这种病变似乎更加普遍和明显。由视神经管狭窄引起的进行性视神经病变可能是 JMC 的特征之一,而 OCT GCA 可以作为视神经管狭窄情况下视神经病变进展的有效生物标志物。我们建议,JMC 患者应定期进行眼科检查,包括色觉、OCT、视野测试、眼眶和颅面成像。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
JBMR Plus
JBMR Plus Medicine-Orthopedics and Sports Medicine
CiteScore
5.80
自引率
2.60%
发文量
103
审稿时长
8 weeks
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