A study of clinical spectrum of pseudo exfoliation syndrome

Dr. Chimata Triveni, D. Divya, Dr. N. Lakshmi, D. Sirisha
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Abstract

Background: Pseudoexfoliation syndrome (PXS) is the most common identifiable cause of secondary glaucoma, the prevalence of which varies considerably among different (PXF) ethnicities. Pseudoexfoliation is a genetically inherited condition. The prevalence of pseudoexfoliation increases with age. It is a common condition in the elderly population. This study aimed to assess the prevalence of and complications in patients with pseudo-exfoliation. Methods: This is an observational study performed in a sample of 103 patients (112 eyes) with pseudo-exfoliation for one year from October 2017-September-2018. Patients visiting the Ophthalmology department, NRI General Hospital, Chinakakani were enrolled in this study. Detailed evaluation including ophthalmic and general history, slit lamp biomicroscope, intraocular pressure measurement, gonioscopy and detailed eye examination was performed in all patients. Results: A total of 103 patients were analyzed; the major age group was 71-80 (40.78%). Among the Male patients were found to be more (66.02%). Majority of the patients were affected unilaterally (91.26%) and remaining bilaterally (8.24%). On slit-lamp examination degranulation of pupillary ruff and pseudoexfoliation material on the anterior capsule of the lens were present in 59.82% and 52.70% whereas corneal endothelium pigments, iris transillumination defects and pigments on the anterior lens capsule were absent in 82.1%, 91.1% and 68.80% respectively. All the cases were identified with PXF material on pupillary margin of the iris. Majority of the patients (72.32%) had normal intraocular pressure. Glaucoma and ocular hypertension were seen in 20.53% and 7.14% of eyes. On gonioscopy, pseudoexfoliation material in the angle, pigments and sampaolesi’s line were identified in 27.7%, 63.4% and 43.80% respectively. Only 8.69% of eyes had 6/24 or better vision, while 8.69% had perception of light (PL) to No perception of light in PXF Glaucoma patients. Conclusion: The study concluded the need for early diagnosis and various complications involved in pseudoexfoliation.
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假性脱落综合征临床谱的研究
背景:假脱落综合征(PXS)是继发性青光眼最常见的可识别原因,其患病率在不同(PXF)种族之间差异很大。假角质脱落是一种遗传性疾病。假性脱落的患病率随着年龄的增长而增加。这是老年人的常见病。本研究旨在评估假性去角质患者的患病率和并发症。方法:这是一项观察性研究,从2017年10月至2018年9月,对103例(112只眼睛)进行假去角质手术。本研究选取了在Chinakakani NRI总医院眼科就诊的患者。对所有患者进行详细的评估,包括眼科和一般病史、裂隙灯生物显微镜、眼压测量、角膜镜检查和详细的眼部检查。结果:共分析103例患者;年龄以71 ~ 80岁为主(40.78%)。以男性患者居多(66.02%)。大多数患者单侧发病(91.26%),其余患者双侧发病(8.24%)。裂隙灯检查发现,晶状体前囊有脱粒和假脱落物质,分别占59.82%和52.70%,而角膜内皮色素、虹膜透照缺损和晶状体前囊无色素分别占82.1%、91.1%和68.80%。所有病例均在虹膜瞳孔边缘检测到PXF物质。大多数患者(72.32%)眼压正常。青光眼和高眼压分别占20.53%和7.14%。角、色素和sampaolesi线的假脱落物质检出率分别为27.7%、63.4%和43.80%。PXF型青光眼患者只有8.69%的眼睛有6/24及以上的视力,8.69%的患者有光感(PL)至无光感。结论:早期诊断假性去角质的必要性及各种并发症。
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