年轻女性微球眼伴非典型颞虹膜缺损。

IF 0.6 Q3 MEDICINE, GENERAL & INTERNAL
Aahan Shah, Subashini Kaliaperumal, Mary Stephen, Keerthana Ramachandran
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引用次数: 0

摘要

微球晶状体是一种罕见的先天性晶状体异常,其特征是晶状体前后厚度增加,赤道直径减小,使晶状体呈球形。虹膜缺损,通常累及鼻间虹膜,由胎儿裂隙闭合不完全引起。据我们所知,这是第一例双侧非典型(颞)虹膜缺损伴微球眼球畸形的病例。一个早期的青少年患者接受了多重先天性异常综合征的评估。眼科检查发现双侧瞳孔边缘颞叶切口,结缔组织完整,提示结缔组织瘤和强色素晶状体小带伴白内障。其他发现包括腹股沟疝、黏膜下腭裂、二尖瓣脱垂、小头畸形和高度近视。治疗的重点是眼镜和定期眼压监测,因为保持了视力。该病例强调了可能的结缔组织疾病的可变表现,具有非典型的眼部特征,如微球眼、颞虹膜缺损和晶状体半脱位。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Microspherophakia with an atypical temporal iris coloboma in a young female.

Microspherophakia is a rare congenital lens abnormality characterised by increased anterior-posterior thickness and reduced equatorial diameter, giving the lens a spherical shape. Iris coloboma, typically involving the inferonasal iris, results from incomplete fetal fissure closure. To our knowledge, this is the first reported case of microspherophakia with bilateral atypical (temporal) iris coloboma. An early adolescent patient underwent a syndromic evaluation for multiple congenital anomalies. Ophthalmological examination revealed bilateral temporal notches of the pupillary rim with intact collarettes, suggesting coloboma and strongly pigmented lens zonules with phacodonesis. Additional findings included inguinal hernia, submucosal cleft palate, mitral valve prolapse, microcephaly and high myopia. Management focused on glasses and periodic intraocular pressure monitoring due to preserved visual acuity. This case underscores the variable presentation of probable connective tissue disorders, with atypical ocular features like microspherophakia, temporal iris coloboma and lens subluxation.

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来源期刊
BMJ Case Reports
BMJ Case Reports Medicine-Medicine (all)
CiteScore
1.40
自引率
0.00%
发文量
1588
期刊介绍: BMJ Case Reports is an important educational resource offering a high volume of cases in all disciplines so that healthcare professionals, researchers and others can easily find clinically important information on common and rare conditions. All articles are peer reviewed and copy edited before publication. BMJ Case Reports is not an edition or supplement of the BMJ.
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