Congenital oesophageal web or ring (Q46316)

From determinar.ia.br - Determine suas informações
Revision as of 14:49, 13 August 2026 by Determinaradmin (talk | contribs) (‎Changed an Item)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
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.
Language Label Description Also known as
default for all languages
LB12.0
    English
    Congenital oesophageal web or ring
    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.

      Statements

      CID11:LB12.0
      0 references
      dki-india-LB12.0
      0 references
      Concluído
      0 references
      13 August 2026
      0 references
      0 references