ICD·index Chapters ENESDE
LB12.0 category

Congenital oesophageal web or ring

Definition

A rare form of incomplete oesophageal obstruction due to a developmental defect of the primitive foregut that presents as a mucosal lesion forming an incomplete diaphragm. Symptoms (apparent from birth) include dysphagia, regurgitation, and choking.

Exclusions

Also indexed as

Congenital Schatzki ringCongenital oesophageal web or ringCongenital ring of oesophagusCongenital web of oesophaguscongenital webbed oesophagus

Nearby in Structural developmental anomalies of oesophagus