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Patient Story

A 4-month-old infant presents to your office with noisy breathing. His mother notes it began at a few weeks of life and has gradually worsened. The noise is described as a high-pitched wheeze with inspiration. It worsens when the baby is feeding, crying, or supine. Laryngoscopy confirms the diagnosis of laryngomalacia (Figure 31-1). The infant is treated with acid suppression therapy. The infant--rsquo;s symptoms resolve by 18 months of age.


Multiple views of laryngomalacia in one infant. Note the omega-shaped epiglottis and prolapse of redundant supraglottic tissue into the airway. (Used with permission from Paul Krakovitz, MD.)


Laryngomalacia is a congenital abnormality of the larynx. It results in dynamic collapse of supraglottic structures leading to airway obstruction.


Laryngomalacias, Larynx chondromalacia.


  • Most common cause of stridor in newborns, affecting 45 to 75 percent of all infants with congenital stridor.1

Etiology and Pathophysiology

  • Exact etiology of laryngomalacia is unknown.

  • Theories include anatomic displacement of flaccid tissue, immaturity of cartilage, neurologic underdevelopment affecting laryngeal function, and tone.1

Risk Factors

  • Gastroesophageal and laryngopharyngeal reflux.

  • Neurologic disease.

  • Secondary airway lesions.

  • Congenital heart disease.

  • Congenital abnormalities/genetic disorders.


Clinical Features

  • Presents with inspiratory stridor that typically worsens with feeding, crying, supine, or positioning.

  • Symptoms begin within first few weeks of life, peak at 6 to 8 months, and usually resolve by 12 to 24 months.

  • Common associated symptoms include regurgitation, coughing, choking, and slow feeding.

  • Less common symptoms include respiratory distress, cyanosis, pectus excavatum, and failure to thrive.


  • Diagnosis suspected by clinical history and confirmed by awake dynamic flexible laryngoscopy.

  • Typical features include supraglottic tissue prolapse during inspiration, omega-shaped epiglottis, retroflexed epiglottis, foreshortened aryepiglottic folds, and redundant arytenoid tissue (Figure 31-1).

  • Based on history, patients may need to be screened for secondary, synchronous airway lesions.

Laboratory Testing and Imaging

  • Usually not indicated. If there is concern for a synchronous airway lesion, may consider bronchoscopy or imaging.

Differential Diagnosis

  • Subglottic stenosis--mdash;Congenital or acquired narrowing of the subglottic airway (Figure 31-2).

  • Tracheomalacia--mdash;Flaccidity of tracheal cartilage leading to tracheal collapse especially with increased airflow (Figure 31-3).

  • Vocal cord paresis or paralysis--mdash;Weakness or immobility of one or both vocal cords (Figure 31-4).


Subglottic stenosis. Note the true vocal cords laterally and the area of airway narrowing seen just distally in the subglottis. (Used with permission ...

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