A Case of Congenital Bilateral Anophthalmia.

Current health sciences journal Pub Date : 2024-04-01 Epub Date: 2024-06-30 DOI:10.12865/CHSJ.50.02.20
Fatema Alhubaishi, Aysha Almedfaa, Mehryar Andacheh
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Abstract

Introduction: Anophthalmia and microphthalmia are orbito-facial developmental disorders characterized by deficient growth and impaired visual capability [1]. These rare disorders may be unilateral or bilateral. Congenital anophthalmia is the complete absence of the eye [2, 3]. The prevalence of both conditions is estimated at 0.2-3 per 10,000 births [4]. We report a case of congenital bilateral anophthalmia that was undetected during follow-up but diagnosed after birth.

Case description: 24-year-old Bahraini female, who is not a known case of any medical illnesses, primigravida at 39+6 weeks of gestation gave birth to a live male baby via vacuum extraction delivery due to recurrent variable decelerations and poor maternal effort. On physical examination, bilateral anophthalmia was immediately observed. No other anomalies were detected. The investigations ordered were MRI brain and orbit, which showed: Absence of bilateral eye globes-features of bilateral anophthalmia. We advised the parents the baby will need socket expansion/ conformer placement to maintain facial symmetry and cosmetic outcome with neurocognitive and development assessment every 2 months as well as speech and language evaluation.

Conclusion: Although many probable factors leading to anophthalmia are suggested, many cases arise idiopathically. Due to the nature of the defect, oftentimes prenatal diagnosis with routine scans is challenging. Therefore, more research into probable causes will prompt the healthcare professional to use more sensitive studies to detect the anomaly prenatally to potentially reduce the psychological and financial impact on the parents.

一例先天性双侧无眼球症。
导言:无眼球症和小眼球症是一种眶面发育障碍性疾病,其特点是发育不良和视觉能力受损[1]。这些罕见的疾病可能是单侧的,也可能是双侧的。先天性无眼症是指完全没有眼球[2, 3]。这两种疾病的发病率估计为每万名新生儿中 0.2-3 例 [4]。我们报告了一例先天性双侧无眼球症病例,该病例在随访期间未被发现,但在出生后被确诊。病例描述:24 岁巴林籍女性,无任何内科疾病,初产妇,妊娠 39+6 周,因反复出现不同程度的减速和产妇用力不足,通过真空吸引分娩生下一名男婴。体格检查时,立即观察到双侧无眼球。没有发现其他异常。医生要求进行脑部和眼眶核磁共振检查,结果显示双侧眼球缺失--双侧无眼球特征。我们建议孩子的父母为孩子进行内眦赘皮扩张术/保形器置入术,以保持面部对称和美观,并每两个月进行一次神经认知和发育评估以及言语和语言评估:尽管导致无眼症的可能因素很多,但许多病例都是特发性的。由于这种缺陷的性质,常规扫描的产前诊断往往具有挑战性。因此,对可能的病因进行更多的研究将促使医护人员使用更敏感的研究来检测产前异常,从而减少对父母的心理和经济影响。
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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