Literature DB >> 31891841

Temporal bone and intracranial abnormalities in syndromic causes of hearing loss: an updated guide.

Felice D'Arco1, Adam Youssef1, Evangelia Ioannidou2, Sotirios Bisdas2, Lorenzo Pinelli3, Pablo Caro-Dominguez4, Robert Nash5, Ata Siddiqui6, Giacomo Talenti7.   

Abstract

PURPOSE: To describe in detail the temporal bone and brain findings in both common and rare syndromic causes of hearing loss, with the purpose of broadening among radiologists and enhance the current understanding of distinct imaging features in paediatric patients with syndromic hearing loss.
METHODS: A detailed search of electronic databases has been conducted, including PubMed, Ovid Medline, Scopus, Cochrane Library, Google Scholar, National Institute for Health and Care Excellence (NICE), Embase, and PsycINFO.
RESULTS: Syndromic causes of hearing loss are characterised by different and sometimes specific abnormalities in the temporal bone.
CONCLUSION: A complete knowledge of the image findings in the temporal bones, brain, skull and other body regions is critical for the optimal assessment and management of these patients.
Copyright © 2020 The Authors. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Brain malformations; Head and neck radiology; Inner ear malformations; Pediatric radiology; Syndromic hearing loss

Year:  2019        PMID: 31891841     DOI: 10.1016/j.ejrad.2019.108803

Source DB:  PubMed          Journal:  Eur J Radiol        ISSN: 0720-048X            Impact factor:   3.528


  3 in total

1.  Guidelines for magnetic resonance imaging in pediatric head and neck pathologies: a multicentre international consensus paper.

Authors:  Felice D'Arco; Livja Mertiri; Pim de Graaf; Bert De Foer; Katarina S Popovič; Maria I Argyropoulou; Kshitij Mankad; Hervé J Brisse; Amy Juliano; Mariasavina Severino; Sofie Van Cauter; Mai-Lan Ho; Caroline D Robson; Ata Siddiqui; Steve Connor; Sotirios Bisdas
Journal:  Neuroradiology       Date:  2022-04-23       Impact factor: 2.804

2.  Neuroimaging in Kabuki syndrome and another KMT2D-related disorder.

Authors:  Rachel T Stadelmaier; Margaret A Kenna; Devon Barrett; Thomas E Mullen; Olaf Bodamer; Pankaj B Agrawal; Caroline D Robson; Monica H Wojcik
Journal:  Am J Med Genet A       Date:  2021-08-09       Impact factor: 2.802

3.  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

  3 in total

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