Laryngeal cleft anomalies are rare congenital defects of the posterior lary
ngotracheal. wall that usually present with a history of recurrent respirat
ory tract infections during the early neonatal period. Presentation of type
I clefts can be subtle and subsequently can result in late diagnosis or in
deed failure to present. We report on the case of a type I laryngeal cleft
presenting with a history of recurrent lower respiratory tract infections a
nd severe gastro-oesphageal reflux disease, at 19 years of age. This is the
oldest documented initial presentation of a congenital laryngeal cleft, an
d emphasizes the importance of maintaining a suspicion of the diagnosis int
o early adulthood. We further highlight the role of gastro-oesophageal refl
ux disease in the presentation of laryngeal clefts.