后小眼色素视网膜病变综合征。

IF 1.6 Q3 OPHTHALMOLOGY Journal of Ophthalmic & Vision Research Pub Date : 2023-04-01 DOI:10.18502/jovr.v18i2.13190
Syed Saifuddin Adeel, Syed Mohideen Ka, Anuj Sharma, Vinit J Shah, Adheesh Shetty
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引用次数: 0

摘要

目的:报告一例47岁女性后小眼色素视网膜病变综合征(PMPRS),并对文献进行简要回顾。病例报告:一名47岁女性,有视力缺陷史并伴有夜视困难。临床检查包括全面的眼部检查,显示眼底弥漫性色素斑斑,眼部生物测量显示轴长短,前节尺寸正常,视网膜电图显示消失反应,光学相干断层扫描显示凹裂,超声显示巩膜-脉络膜复合体增厚。研究结果与其他PMPRS作者报告的结果一致。结论:高度远视患者应怀疑有或无其他眼部和全身相关的后小眼。必须在就诊时仔细检查患者,并密切随访以保持视觉功能。
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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Posterior Microphthalmos Pigmentary Retinopathy Syndrome.

Purpose: To report a case of a rare disease entity Posterior Microphthalmos Pigmentary Retinopathy Syndrome (PMPRS) in a 47-year-old female with a brief review of literature.

Case report: A 47-year-old woman presented with a history of defective vision with an associated difficulty in night vision. Clinical workup was done, which included a thorough ocular examination showing diffuse pigmentary mottling of fundus, ocular biometry showing short axial length with normal anterior segment dimensions, electroretinography showing extinguished response, optical coherence tomography showing foveoschisis, and ultrasonography showing thickened sclera-choroidal complex. Findings were consistent with those reported by other authors with PMPRS.

Conclusion: Posterior microphthalmia with or without other ocular and systemic associations should be suspected in cases with high hyperopia. It is mandatory to carefully examine the patient at presentation and close follow-ups are needed to maintain visual function.

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来源期刊
CiteScore
3.60
自引率
0.00%
发文量
63
审稿时长
30 weeks
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