一名尼日利亚青少年的马歇尔综合症表现为屈光不正

O. Ogun, O. Adediran, A. Ashaye, O. Nwaorgu
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引用次数: 0

摘要

一名14岁的女孩,因从小视力不佳而来到我们的眼科诊所。高度近视伴视网膜退行性病变。然而,颅面畸形和骨骼畸形以及听力障碍引起临床怀疑为单一的多系统疾病,促使文献回顾,支持马歇尔综合征(MS)的临床诊断。本病例报告和文献回顾描述了MS,值得注意的是其罕见性,遗传基础和独特的表型特征,但在常规临床实践中容易被忽视。这是西非报告的第二例多发性硬化症病例,第一例发生在一名尼日利亚妇女身上。这种极其罕见的全身性疾病可能出乎意料地出现,作为一种看似常见的屈光不正,很容易被忽视,没有高度的怀疑。然而,准确的诊断是很重要的,因为多发性硬化症需要多学科团队的合作管理,而不仅仅是眼科医生,以确保良好的生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Marshall syndrome in a Nigerian teenager presenting with refractive error
A 14-year-old girl, presented to our eye clinic, with poor distance vision since childhood. High myopia with degenerative retina was found. However, craniofacial disproportion and skeletal dysmorphism, as well as hearing impairment, drew clinical suspicion for a single multisystemic disorder prompting a literature review, which supported a clinical diagnosis of Marshall syndrome (MS). This case report and review of literature describes MS, worthy of note for its rarity, genetic basis and distinctive phenotypic features, but yet easily overlooked in routine clinical practice. This is the second case of MS reported in West Africa and the first in a Nigerian female. This extremely rare, systemic disorder may present unexpectedly, as a seemingly common condition as a refractive error and can be easily overlooked, without a high index of suspicion. Accurate diagnosis, however, is important because MS requires collaborative management by a multidisciplinary team and not the ophthalmologist alone, to ensure a good quality of life.
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