Isolated congenital facial nerve agenesis.

IF 0.5 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING BJR Case Reports Pub Date : 2023-05-01 DOI:10.1259/bjrcr.20220119
Amarit Kay Gill, Ashok Raghavan, Eishaan Kamta Bhargava
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Abstract

An otherwise healthy 2-month-old boy was referred to ENT for a congenital right facial palsy, with a birth history of difficult ventouse delivery. Initially, a traumatic cause was suspected, however subsequent MR 3D-FIESTA (T2 weighted) imaging demonstrated a right facial nerve agenesis with normal appearances of the remainder of the brain parenchyma, cranial nerves and parotid glands. There were no syndromic features or hearing difficulties. Isolated congenital nerve agenesis is a rare condition, with very few case reports available in the literature. Pre-natal 4D ultrasound imaging further supports the diagnosis. To our knowledge, this is the first published pre-natal ultrasound image of congenital facial nerve palsy. The infant has been referred for consideration of nerve reconstruction surgery, and is receiving multi-disciplinary input from ENT, Physiotherapy and Ophthalmology, the latter for prevention of exposure keratitis.

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孤立性先天性面神经发育不全。
一个健康的2个月大的男孩被转介到耳鼻喉科先天性右面瘫,有困难的出生史静脉分娩。最初,怀疑是外伤性原因,但随后的MR 3D-FIESTA (T2加权)成像显示右侧面神经发育不全,其余脑实质、颅神经和腮腺外观正常。没有综合征特征或听力障碍。孤立性先天性神经发育不全是一种罕见的疾病,文献中很少有病例报告。产前4D超声成像进一步支持诊断。据我们所知,这是首次发表的先天性面神经麻痹的产前超声图像。该婴儿已被转介考虑神经重建手术,并正在接受耳鼻喉科、物理疗法和眼科的多学科投入,后者用于预防暴露性角膜炎。
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BJR Case Reports
BJR Case Reports RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING-
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审稿时长
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