Fraser syndrome with extremely rare features of unilateral anophthalmia and penile torsion in an Afghan neonate: A case report

Turyalai Hakimi , Mansoor Aslamzai
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Abstract

Background

Fraser syndrome is a very rare genetic disorder with multiple organ-system abnormalities. The diagnosis is usually made on the basis of clinical examination, and management requires a multidisciplinary approach.

Case Presentation

We present a case of Fraser syndrome with very rare manifestations of unilateral anophthalmia and moderate penile torsion in an Afghan neonate who was born to a 16-year-old mother. Physical findings and a CT scan of the brain and eyes were used to diagnose the aforementioned syndrome. The surgical repairs of cryptophthalmos and penile torsion were planned to be performed after infancy, and the baby was discharged in good health.

Conclusion

Anophthalmia and penile torsion are very rare components of Fraser syndrome. Very young maternal age may play a predisposing role in the pathogenesis of Fraser syndrome. The multiple organ defects in Fraser syndrome make this entity more challenging to deal with, particularly in low-resourced settings.
弗雷泽综合征与极其罕见的特征单侧眼失和阴茎扭转在阿富汗新生儿:一个案例报告
弗雷泽综合征是一种非常罕见的遗传性疾病,伴有多器官系统异常。诊断通常是在临床检查的基础上做出的,治疗需要多学科的方法。病例介绍我们提出一个病例弗雷泽综合征非常罕见的表现单侧无眼和中度阴茎扭转在阿富汗新生儿谁是由一个16岁的母亲所生。物理检查和CT扫描的大脑和眼睛被用来诊断上述综合征。隐眼和阴茎扭转的手术修复计划在婴儿期后进行,婴儿健康出院。结论无眼和阴茎扭转是弗雷泽综合征的罕见症状。非常年轻的母亲年龄可能在弗雷泽综合征的发病机制中起易感作用。弗雷泽综合征的多器官缺陷使该实体更具挑战性,特别是在资源匮乏的环境中。
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来源期刊
Global pediatrics
Global pediatrics Perinatology, Pediatrics and Child Health
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