Skip to content
Research Article Open access CC BY 4.0

A Female Case of Goldenhar Syndrome with Mandibular Hypoplasia and Aural Involvement

F. Ferrari, F. D’Orazio, L. Patriarca, A. Piccorossi, S. Di Fabio, A. Barile, E. Di Cesare, A. Splendiani

Journal of Advances in Medicine and Medical Research · pp. 1–5 · Published 17 Oct 2015

10.9734/BJMMR/2016/21666

Abstract

Goldenhar syndrome (GS) is a poly-malformation syndrome, also defined as oculo-auricolo-vertebral dysplasia with hemifacial microsomia. It is a rare congenital defect involving first and second branchial arches. The aetiology is not known. The most supported hypothesis is based on the abnormal embryonic vascular supply after mesodermal migration. Autosomal dominant, autosomal recessive and multifactorial modes of inheritance have been reported. We report the case of a female neonate affected by hemifacial microsomia and presence of pre-auricular tragi. Patients were subjected to computed tomography scan and MRI that revealed a mandibular unilateral hypoplasia without association of skeleton, brain and ocular alteration. The purpose of our study was to define the important role of the CT and MRI in the diagnosis of this poly-marformation syndrome. 

Goldenhar syndrome (GS) magnetic resonance computed tomography oculo-auriculo-vertebral dysplasia hemifacial microsomia pre-auricular tragi.

Cited by 1

Goldenhar Syndrome: A Case Report

Ruby Kurniawan, I. Kadek Suarca, I. W. Suryawan · Open Access Macedonian Journal of Medical Sciences · 2019

Article metrics

Real usage data collected on this platform.

28

Page views

0

PDF downloads

4

Outbound clicks

1

Citations

Views over time

Views by country

Approximate, from request IP at view time — not citizenship or institution. Countries with fewer than 5 views are grouped as "Other".

Traffic sources

Referring site, by host.

Views and downloads exclude known bots/crawlers. Citations combines this platform's own DOI-resolved index with each external source's own reported total — see Cited by above for individually listed citing works. Last refreshed 0 seconds ago.