Multiple congenital anomalies associated with infantile achalasia
- PMID: 7418990
- DOI: 10.1007/BF01888634
Multiple congenital anomalies associated with infantile achalasia
Abstract
Achalasia is rare in the pediatric age group, particularly in the neonate and young infant. The symptoms are often nonspecific and may not even suggest a primary esophageal disorder. This is a report of two cases of achalasia seen in neonates, both of whom has other unusual and exceedingly uncommon congenital abnormalities.