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. 1991 Nov;66(11):1353–1354. doi: 10.1136/adc.66.11.1353

Familial infantile oesophageal achalasia.

T K Kaar 1, R Waldron 1, M S Ashraf 1, J B Watson 1, M O'Neill 1, W O Kirwan 1
PMCID: PMC1793307  PMID: 1755653

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.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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