Laryngeal cleft, first described by Richter in 1792, is a rarecongenital malformation.
Diagnosis can be challenging and is contingent upon a high index of suspicion based on …

Objective To review the presentation and associated congenital abnormalities of laryngeal
cleft and present guidelines for its evaluation and management. Design A 10-year …

Objectives Review the latest diagnostic and treatment modalities for laryngeal and
laryngotracheoesophageal clefts as they can be a major cause of respiratory and feeding …

OBJECTIVE: To review the clinical presentation and management of all infants and children
presenting with laryngeal clefts to a tertiary pediatric ENT centre and to identify changes in …

Introduction: Traditionally, small laryngeal clefts may be closed endoscopically, while larger
clefts necessitate an open anterior approach. We report the presentation, evaluation and …

Introduction Laryngeal clefts (LC) are congenital malformations of the upper aerodigestive
tract that can cause dysphagia, aspiration, and subsequent pulmonary complications. This …

Background Laryngeal cleft (LC) is a rare congenital anomaly manifesting in a variety of
symptoms, including swallowing disorders and aspirations, dyspnea, stridor and …

Objective To review the presentation and evaluation of laryngotracheoesophageal clefts as
well as their treatment modalities, especially endoscopic closure. Study design retrospective …

Introduction Laryngeal cleft is a congenital condition in which an opening in the posterior
laryngotracheal wall allows food and liquid to pass from the esophageal lumen to the airway …

OBJECTIVES: To report our experience with all patients diagnosed with type 1 laryngeal
cleft over a period of 3 years in our referral practice and to describe a functional diagnostic …