Literature DB >> 30385470

The Unwound Cochlea: A Specific Imaging Marker of Branchio-Oto-Renal Syndrome.

A Hsu1, N Desai1, M J Paldino2.   

Abstract

BACKGROUND AND
PURPOSE: Branchio-oto-renal syndrome is an important syndromic cause of hearing loss. Our aim was to determine the test characteristics of the unwound cochlea on temporal bone CT for the diagnosis of branchio-oto-renal syndrome in a cohort of children with hearing loss.
MATERIALS AND METHODS: Patients were identified retrospectively with a clinical diagnosis of branchio-oto-renal syndrome and CT imaging of the temporal bones. Age-matched controls were also identified with sensorineural hearing loss not related to a diagnosis of branchio-oto-renal syndrome and CT imaging of the temporal bones. All examinations were reviewed by 2 neuroradiologists blinded to the diagnosis of branchio-oto-renal syndrome versus controls for the absence/presence of an unwound cochlea defined as anteromedial rotation and displacement of the middle and apical turns away from the basal turn.
RESULTS: The final study group comprised 9 patients with branchio-oto-renal syndrome (age range, 1-14 years; mean age, 8.0 ± 4.3 years) and 50 control patients (age range, 1-16 years; mean age, 7.9 ± 4.1 years). The cochlea was subjectively abnormal in all 9 patients. In 8 patients (89%), imaging demonstrated a typical unwound cochlear morphology. By contrast, none of the control subjects demonstrated an unwound cochlea on either side. Statistically, the unwound cochlea was significantly more frequent in the branchio-oto-renal group compared with controls (P < .001). The unwound cochlea was 89% sensitive and 100% specific for the diagnosis of branchio-oto-renal syndrome.
CONCLUSIONS: The unwound cochlea is a specific imaging marker of branchio-oto-renal syndrome. These findings further support the diagnostic accuracy and therefore the utility of temporal bone imaging in the diagnosis of this disorder.
© 2018 by American Journal of Neuroradiology.

Entities:  

Mesh:

Year:  2018        PMID: 30385470     DOI: 10.3174/ajnr.A5856

Source DB:  PubMed          Journal:  AJNR Am J Neuroradiol        ISSN: 0195-6108            Impact factor:   3.825


  6 in total

1.  The link between inner ear malformations and the rest of the body: what we know so far about genetic, imaging and histology.

Authors:  Felice D'Arco; Eser Sanverdi; William T O'Brien; Ajay Taranath; Giacomo Talenti; Susan I Blaser
Journal:  Neuroradiology       Date:  2020-03-03       Impact factor: 2.804

2.  Re-Examining the Cochlea in Branchio-Oto-Renal Syndrome: Genotype-Phenotype Correlation.

Authors:  J Pao; F D'Arco; E Clement; S Picariello; G Moonis; C D Robson; A F Juliano
Journal:  AJNR Am J Neuroradiol       Date:  2022-01-20       Impact factor: 3.825

Review 3.  Anatomical and audiological considerations in branchiootorenal syndrome: A systematic review.

Authors:  Kirsty Biggs; Gemma Crundwell; Christopher Metcalfe; Jameel Muzaffar; Peter Monksfield; Manohar Bance
Journal:  Laryngoscope Investig Otolaryngol       Date:  2022-02-08

4.  Characteristic Cochlear Hypoplasia in Patients with Walker-Warburg Syndrome: A Radiologic Study of the Inner Ear in α-Dystroglycan-Related Muscular Disorders.

Authors:  G Talenti; C Robson; M S Severino; C A Alves; D Chitayat; H Dahmoush; L Smith; F Muntoni; S I Blaser; F D'Arco
Journal:  AJNR Am J Neuroradiol       Date:  2020-10-29       Impact factor: 3.825

Review 5.  Radiological diagnosis of the inner ear malformations in children with sensorineural hearing loss.

Authors:  Bernadine Quirk; Adam Youssef; Mario Ganau; Felice D'Arco
Journal:  BJR Open       Date:  2019-06-14

6.  Phenotype-genotype correlation in patients with typical and atypical branchio-oto-renal syndrome.

Authors:  Masatsugu Masuda; Ayako Kanno; Kiyomitsu Nara; Hideki Mutai; Naoya Morisada; Kazumoto Iijima; Noriko Morimoto; Atsuko Nakano; Tomoko Sugiuchi; Yasuhide Okamoto; Sawako Masuda; Sayaka Katsunuma; Kaoru Ogawa; Tatsuo Matsunaga
Journal:  Sci Rep       Date:  2022-01-19       Impact factor: 4.379

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.