[HTML][HTML] Hearing impairment and ear anomalies in craniofacial microsomia: a systematic review

W Rooijers, PAE Tio, MP van der Schroeff… - International Journal of …, 2022 - Elsevier
The aim of this systematic review was to review the literature on hearing impairment and ear
anomalies in patients with craniofacial microsomia and to determine their prevalence. Sixty …

Genetics of inner ear malformations: a review

D Brotto, F Sorrentino, R Cenedese, I Avato, R Bovo… - Audiology …, 2021 - mdpi.com
Inner ear malformations are present in 20% of patients with sensorineural hearing loss.
Although the first descriptions date to the 18th century, in recent years the knowledge about …

Neurocristopathies: Enigmatic appearances of neural crest cell–derived abnormalities

TS Sato, A Handa, S Priya, P Watal, RM Becker… - Radiographics, 2019 - pubs.rsna.org
The neural crest is an important transient structure that develops during embryogenesis in
vertebrates. Neural crest cells are multipotent progenitor cells that migrate and develop into …

Syndromic hearing loss in children

M Lewis, CD Robson, DA Felice - Neuroimaging …, 2023 - neuroimaging.theclinics.com
The estimated prevalence of permanent bilateral hearing loss (HL) in children is 1.33 per
1000 live births, increasing to 3.5 per 1000 adolescents, presumably reflecting additional …

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

F D'Arco, A Youssef, E Ioannidou, S Bisdas… - European Journal of …, 2020 - Elsevier
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 …

[HTML][HTML] Benefits of bone conduction hearing aid in children with unilateral aural atresia

D Brotto, F Sorrentino, D Cazzador… - Acta …, 2023 - ncbi.nlm.nih.gov
Objective To assess the hearing benefit with a unilateral bone conduction hearing aid in a
cohort of children with unilateral aural atresia. Methods Cross-sectional case series pilot …

[HTML][HTML] A decade of clinical research on clinical characteristics, medical treatments, and surgical treatments for individuals with craniofacial microsomia: What have …

RW Renkema, CJJM Caron, CL Heike… - Journal of Plastic …, 2022 - Elsevier
Aim This article provides a review of a decade of clinical research studies on clinical
features, medical interventions, and surgical interventions for individuals with craniofacial …

The spectrum of cochlear malformations in CHARGE syndrome and insights into the role of the CHD7 gene during embryogenesis of the inner ear

MA Lewis, A Juliano, C Robson, E Clement, R Nash… - Neuroradiology, 2023 - Springer
Purpose We reviewed the genotypes and the imaging appearances of cochleae in CHARGE
patients from two large tertiary centres and analysed the observed cochlear anomalies …

Oculo-auriculo-vertebral spectrum associated with aberrant subclavian artery in an infant with recurrent respiratory distress

AR Pereira, CHP Grangeiro, LC Pereira… - Revista Paulista de …, 2021 - SciELO Brasil
Objective: To describe an infant with craniofacial microsomia and recurrent respiratory
distress associated with aberrant right subclavian artery in order to review its most frequent …

Three-dimensional analysis of the temporal bone morphology in patients with craniofacial microsomia

X Li, W Liu, X Tang, C Li… - The Cleft Palate …, 2024 - journals.sagepub.com
Objective To characterise the morphology of temporal bone in patients with craniofacial
microsomia (CFM). Design A retrospective study. Setting A craniofacial centre. Patients …