Abstract
Tracheal malformations consist of a variety of anomalies related to abnormal development of the tracheobronchial tree. The most common clinical findings associated with tracheal narrowing include biphasic stridor with a prolonged expiratory component and cough that can be wet or bronchial in nature (from retained secretions). This chapter focuses on tracheomalacia, tracheal stenosis, tracheoesophageal fistula, tracheal bronchus, and bronchogenic cysts.
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Zur, K.B. (2014). Congenital Malformations of the Trachea. In: Elden, L., Zur, K. (eds) Congenital Malformations of the Head and Neck. Springer, New York, NY. https://doi.org/10.1007/978-1-4419-1714-0_7
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DOI: https://doi.org/10.1007/978-1-4419-1714-0_7
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