Esophageal motility in an adult with a congenital H-type tracheoesophageal fistula

Richard F. Heitmiller, Parviz Nikoomanesh, William J. Ravich

Research output: Contribution to journalArticlepeer-review


Congenital H-type tracheoesophageal fistulas (TEF) are rare. Long-standing respiratory symptoms are the most common presenting complaints. Patients with these fistulas have a congenital esophageal motor abnormality characterized by uncoordinated, low-amplitude peristalsis of the esophagal body; both low and normal lower esophageal sphincter pressures have been described. These findings persist despite fistula repair. A case history of an adult patient with congenital TEF is presented and the literature is reviewed. This patient is unusual in that esophageal symptoms (dysphagia) were more prominent than the usual respiratory symptoms.

Original languageEnglish (US)
Pages (from-to)138-141
Number of pages4
Issue number3
StatePublished - Sep 1 1990


  • Achalasia
  • Deglutition
  • Tracheoesophageal fistula
  • disorders

ASJC Scopus subject areas

  • Otorhinolaryngology
  • Gastroenterology
  • Speech and Hearing


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