Literature DB >> 15891641

Inner ear abnormalities in patients with Goldenhar syndrome.

Sotirios Bisdas1, Minoo Lenarz, Thomas Lenarz, Hartmut Becker.   

Abstract

OBJECTIVE: The objective of this study is to investigate the inner ear malformations in patients with Goldenhar syndrome and to hypothesize the potential embryopathogenesis of these malformations. STUDY
DESIGN: Retrospective case review.
SETTING: Tertiary referral center. PATIENTS: Fourteen patients with Goldenhar syndrome.
INTERVENTIONS: Each patient underwent hearing tests and high-resolution computed tomography (CT) of the temporal bone. In six patients, magnetic resonance imaging of the temporal bone also was performed.
RESULTS: Among the 14 patients with Goldenhar syndrome, 13 had outer and middle ear anomalies and 5 (36%) had inner ear malformations, including one case of common cavity.
CONCLUSIONS: Our observations regarding inner ear anomalies in Goldenhar syndrome correlate with the reported cases in the literature and may help to hypothesize the embryological origin of these malformations, which can caused by an early developmental arrest in the fourth gestational week. Specialists evaluating patients with Goldenhar syndrome should be aware of the possibility of inner ear malformations, which could be diagnosed earlier with appropriate imaging studies.

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Mesh:

Year:  2005        PMID: 15891641     DOI: 10.1097/01.mao.0000169796.83695.56

Source DB:  PubMed          Journal:  Otol Neurotol        ISSN: 1531-7129            Impact factor:   2.311


  8 in total

1.  Prenatal evaluation of the middle ear and diagnosis of middle ear hypoplasia using MRI.

Authors:  Eldad Katorza; Catherine Nahama-Allouche; Vanina Castaigne; Marie Gonzales; Eva Galliani; Sandrine Marlin; Jean-Marie Jouannic; Jonathan Rosenblatt; Hubert Ducou le Pointe; Catherine Garel
Journal:  Pediatr Radiol       Date:  2010-12-08

2.  Ectopic external auditory canal and ossicular formation in the oculo-auriculo-vertebral spectrum.

Authors:  Nucharin Supakul; Stephen F Kralik; Chang Y Ho
Journal:  Pediatr Radiol       Date:  2014-12-06

3.  A locus for autosomal dominant accessory auricular anomaly maps to 14q11.2-q12.

Authors:  Yongjia Yang; Jihong Guo; Zheng Liu; Siyuan Tang; Ningdong Li; Mengrong Yang; Qiong Pang; Feiyue Fan; Juan Bu; Song Tao Yuan; Xiangjun Xiao; Yuxiang Chen; Kanxing Zhao
Journal:  Hum Genet       Date:  2006-06-15       Impact factor: 4.132

Review 4.  Congenital hearing impairment.

Authors:  Caroline D Robson
Journal:  Pediatr Radiol       Date:  2006-02-08

5.  A New Model for Congenital Vestibular Disorders.

Authors:  Sigmund J Lilian; Hayley E Seal; Anastas Popratiloff; June C Hirsch; Kenna D Peusner
Journal:  J Assoc Res Otolaryngol       Date:  2018-12-18

6.  Audiological findings in patients with oculo-auriculo-vertebral spectrum.

Authors:  Pricila Sleifer; Natalya de Souza Gorsky; Thayse Bienert Goetze; Rafael Fabiano Machado Rosa; Paulo Ricardo Gazzola Zen
Journal:  Int Arch Otorhinolaryngol       Date:  2014-10-17

Review 7.  Understanding the Pathophysiology of Congenital Vestibular Disorders: Current Challenges and Future Directions.

Authors:  Kenna D Peusner; Nina M Bell; June C Hirsch; Mathieu Beraneck; Anastas Popratiloff
Journal:  Front Neurol       Date:  2021-09-10       Impact factor: 4.003

8.  Ear abnormalities in patients with oculo-auriculo-vertebral spectrum (Goldenhar syndrome).

Authors:  Rafael Fabiano Machado Rosa; Alessandra Pawelec da Silva; Thayse Bienert Goetze; Bianca de Almeida Bier; Sheila Tamanini de Almeida; Giorgio Adriano Paskulin; Paulo Ricardo Gazzola Zen
Journal:  Braz J Otorhinolaryngol       Date:  2011 Jul-Aug
  8 in total

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