Management of Hearing Loss in Patients with Treacher-Collins Syndrome and Hemifacial Microsomia
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Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-030-84733-3_9
Reference12 articles.
1. Marx H. Die Missbildungen des Ohres. In: Henke F, Lubarsh O, editors. Handbuch der Spez Path Anatomie Histologie. Berlin: Springer; 1926. p. 620–5.
2. Rosa F, Coutinho MB, Ferreira JP, Sousa CA. Ear malformations, hearing loss and hearing rehabilitation in children with Treacher Collins syndrome. Acta Otorrinolaringol Esp (English Ed). 2016;67(3):142–7. https://doi.org/10.1016/j.otoeng.2016.05.001.
3. D’Arco F, Youssef A, Ioannidou E, et al. Temporal bone and intracranial abnormalities in syndromic causes of hearing loss: an updated guide. Eur J Radiol. 2020;123(June 2019):108803. https://doi.org/10.1016/j.ejrad.2019.108803.
4. Carvalho GJ, Song CS, Vargervik K, Lalwani AK. Auditory and facial nerve dysfunction in patients with hemifacial microsomia. Arch Otolaryngol Head Neck Surg. 1999;125(2):209–12. https://doi.org/10.1001/archotol.125.2.209.
5. Sleifer P, Gorsky NDS, Goetze TB, Rosa RFM, Zen PRG. Audiological findings in patients with oculo-auriculo-vertebral spectrum. Int Arch Otorhinolaryngol. 2013;19(1):5–9. https://doi.org/10.1055/s-0034-1390137.
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