Abstract
External ear anomalies in Treacher Collins syndrome (TCS) range from preauricular accessory appendages to sinuses to the full spectrum of microtia. These generally occur bilaterally but not necessarily symmetrically. Identification early in life is important for parental reassurance and discussion of future plans.
Up to 85% of TCS patients have microtia or atresia. It is important to present the family with all options of reconstruction, from not intervening to prosthetics and surgical reconstruction. This chapter focuses on the identification and management of external ear anomalies in TCS.
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Alfonso, K.P., Liu, YC.C., Silva, R.C. (2022). Reconstruction of the Ear Deformities Associated with Treacher Collins Syndrome. In: Yates, D.M., Markiewicz, M.R. (eds) Craniofacial Microsomia and Treacher Collins Syndrome. Springer, Cham. https://doi.org/10.1007/978-3-030-84733-3_24
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