| Literature DB >> 1755653 |
T K Kaar1, R Waldron, M S Ashraf, J B Watson, M O'Neill, W O Kirwan.
Abstract
Oesophageal achalasia is uncommon in children and in its familial form it is a rarity. The presentation and management of two male siblings who presented with oesophageal achalasia as infants are reported. A high degree of consanguinity in the parents of the children existed, suggesting autosomal recessive transmission.Entities:
Mesh:
Year: 1991 PMID: 1755653 PMCID: PMC1793307 DOI: 10.1136/adc.66.11.1353
Source DB: PubMed Journal: Arch Dis Child ISSN: 0003-9888 Impact factor: 3.791