8.12 Pediatric Hearing Loss

May 19, 2020 by in OTOLARYNGOLOGY Comments Off on 8.12 Pediatric Hearing Loss

10.1055/b-0038-162799 8.12 Pediatric Hearing Loss Key Features Age at identification has significantly decreased since the advent of newborn hearing screening. Early identification and treatment of hearing loss is essential to…

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8.11 Congenital Nasal Obstruction

May 19, 2020 by in OTOLARYNGOLOGY Comments Off on 8.11 Congenital Nasal Obstruction

10.1055/b-0038-162798 8.11 Congenital Nasal Obstruction Key Features Congenital nasal obstruction can range in severity from a mild irritant to a life-threatening condition with potentially devastating consequences in the neonate. The…

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8.10 Diseases of the Adenoids and Palatine Tonsils

May 19, 2020 by in OTOLARYNGOLOGY Comments Off on 8.10 Diseases of the Adenoids and Palatine Tonsils

10.1055/b-0038-162797 8.10 Diseases of the Adenoids and Palatine Tonsils 8.10.1 Adenotonsillitis Key Features Adenotonsillitis is most commonly viral in etiology. Bacterial etiology is similar to acute otitis media (OM): Group…

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8.9 Genetics and Syndromes

May 19, 2020 by in OTOLARYNGOLOGY Comments Off on 8.9 Genetics and Syndromes

10.1055/b-0038-162796 8.9 Genetics and Syndromes Congenital anomalies, whether single or multiple, can be induced by environmental and teratogenic insults as well as chromosomal or single-gene defects. This chapter includes only…

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8.8 Pierre Robin′s Sequence

May 19, 2020 by in OTOLARYNGOLOGY Comments Off on 8.8 Pierre Robin′s Sequence

10.1055/b-0038-162795 8.8 Pierre Robin′s Sequence Key Features Pierre Robin′s sequence requires the presence of micrognathia, glossoptosis, and usually a cleft palate (frequently U-shaped). Infants present with airway obstruction, because the…

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8.7 Subglottic Stenosis

May 19, 2020 by in OTOLARYNGOLOGY Comments Off on 8.7 Subglottic Stenosis

10.1055/b-0038-162794 8.7 Subglottic Stenosis Key Features The subglottis is the narrowest part of the infant airway. Acquired subglottic stenosis is most commonly found; the most common related factor is intubation….

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8.6 Vascular Rings

May 19, 2020 by in OTOLARYNGOLOGY Comments Off on 8.6 Vascular Rings

10.1055/b-0038-162793 8.6 Vascular Rings Key Features The trachea and esophagus are completely or incompletely surrounded by vascular structures. Compression of the trachea, the bronchi, and/or the esophagus may occur. Most…

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8.5 Tracheoesophageal Fistula and Esophageal Atresia

May 19, 2020 by in OTOLARYNGOLOGY Comments Off on 8.5 Tracheoesophageal Fistula and Esophageal Atresia

10.1055/b-0038-162792 8.5 Tracheoesophageal Fistula and Esophageal Atresia Key Features Tracheoesophageal fistula (TEF) and esophageal atresia (EA) are the result of a congenital communication between the trachea and esophagus. EA is…

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8.4 Laryngeal Clefts

May 19, 2020 by in OTOLARYNGOLOGY Comments Off on 8.4 Laryngeal Clefts

10.1055/b-0038-162791 8.4 Laryngeal Clefts Key Features Laryngeal clefts are a rare congenital anomaly. They are frequently associated with other anomalies. Clinical presentation varies with the extent of the cleft. The…

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8.3 Bilateral Vocal Fold Paralysis

May 19, 2020 by in OTOLARYNGOLOGY Comments Off on 8.3 Bilateral Vocal Fold Paralysis

10.1055/b-0038-162790 8.3 Bilateral Vocal Fold Paralysis Key Features Bilateral vocal fold paralysis is the second most common cause of infantile stridor. It typically requires a tracheotomy for maintenance of airway…

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