Abstract
Congenital ossicular chain abnormalities behind normal ear canal and tympanic membrane are much rarer when compared to conductive hearing loss (CHL) caused by acquired causes. They usually fail neonatal hearing screening tests. It can be diagnosed early if air and bone conduction ABR is done. They usually present as non-progressive hearing loss since birth. If there is an additional sensorineural hearing loss component, they usually present with poor language development. It is seen in cochlear hypoplasia cases. Conductive component is usually due to oval window atresia or stapes footplate fixation. This brings the concept of performing stapedotomy in cases with IEMs. In this chapter, radiological, audiological features, and stapedotomy option in cochlear hypoplasia are presented with case presentations.
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Sennaroglu, L., Bajin, M.D., Cinar, B.C. (2022). Stapedotomy. In: Sennaroglu, L. (eds) Inner Ear Malformations. Springer, Cham. https://doi.org/10.1007/978-3-030-83674-0_14
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DOI: https://doi.org/10.1007/978-3-030-83674-0_14
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