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
- Oesophageal web
(DA20.2)
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
LB12.1Atresia of oesophagusLB12.2Oesophageal fistula without atresiaLB12.3Congenital stenosis or stricture of oesophagusLB12.4Congenital diverticulum of oesophagusLB12.5Congenital dilatation of oesophagus4B4YOther specified diseases of the immune system4B4ZDiseases of the immune system, unspecified