Simultaneous diagnosis of familial achalasia: report of two cases.

Masato HoshinoNobuo OmuraFumiaki YanoSe Ryung YamamotoMinoru MatsudaKatsuhiko Yanaga

Published in: Surgical case reports (2017)

We hereby report on a very rare case of familial achalasia that we experienced which may suggest a genetic element in the onset of achalasia, and reviewed the literature.

Keyphrases

rare case
early onset
systematic review
genome wide
dna methylation