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Isolated congenital facial nerve agenesis.

Authors :
Gill AK
Raghavan A
Bhargava EK
Source :
BJR case reports [BJR Case Rep] 2023 May 15; Vol. 9 (3), pp. 20220119. Date of Electronic Publication: 2023 May 15 (Print Publication: 2023).
Publication Year :
2023

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 ( T <subscript>2</subscript> 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.<br />Competing Interests: Competing interests: No conflicts of interest.<br /> (© 2023 The Authors. Published by the British Institute of Radiology.)

Details

Language :
English
ISSN :
2055-7159
Volume :
9
Issue :
3
Database :
MEDLINE
Journal :
BJR case reports
Publication Type :
Report
Accession number :
37265748
Full Text :
https://doi.org/10.1259/bjrcr.20220119