Branchio‐oto‐renal syndrome with submucous cleft palate: A case report-Reference-Cited by-同舟云学术

Branchio‐oto‐renal syndrome with submucous cleft palate: A case report

Published:2023-06-02 Issue: Volume: Page:
ISSN:1348-8643
Container-title:Oral Science International
language:en
Short-container-title:Oral Science International

Author:

Takaoka Shohei¹^ORCID,Yanagawa Toru²³⁴^ORCID,Kimura Airi⁵,Uchida Fumihiko²^ORCID,Yamagata Kenji²,Bukawa Hiroki²

Affiliation:

1. Department of Oral and Maxillofacial Surgery University of Tsukuba Hospital Tsukuba Ibaraki Japan

2. Department of Oral and Maxillofacial Surgery Institute of Clinical Medicine, Faculty of Medicine, University of Tsukuba Tsukuba Ibaraki Japan

3. Department of Oral and Maxillofacial Surgery Ibaraki Prefectural Central Hospital, Ibaraki Cancer Center, Kasama Ibaraki Japan

4. Center for Medical Education and Training University of Tsukuba Hospital Tsukuba Ibaraki Japan

5. Department of oral and Maxillofacial Surgery, School of Dental Medicine Tsurumi University Yokohama Kanagawa Japan

Abstract

AbstractBackgroundBranchio‐oto‐renal (BOR) syndrome is an autosomal dominant disorder characterized by malformations of the second branchial arch, hearing impairments, and renal anomalies.Case presentationA male infant diagnosed with BOR syndrome presents with an asymmetrical face, forehead protrusion, auricle dysplasia, left external auditory canal closure, hearing impairment, mandibular hypoplasia, submucous cleft palate, facial nerve palsy, renal atrophy, and malalignment of the second toe. Palatoplasty was performed.ConclusionThis case report and related literature review have contributed to existing knowledge regarding BOR syndrome, a rare disorder.

Publisher

Wiley

Subject

Otorhinolaryngology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/osi2.1200

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