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

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

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 …

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 …

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 Diagnosis and treatment of type 1 laryngeal clefts remains a challenge. The
purpose of this study is to determine if early surgical intervention in type I laryngeal clefts …

Laryngeal cleft is a rare pathology and needs a high index of suspicion for diagnosis.
Various classifications are used but the Inglis classification which describes 4 grades of cleft …

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 …

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

Background: Laryngeal clefts are rare congenital anomalies of the upper aerodigestive tract
with a persistent connection between the posterior laryngotracheal airway and the …