Simultaneous diagnosis of familial achalasia: report of two cases

BACKGROUND: Achalasia is a rare disease with a morbidity of 1 in 100,000, for which the exact mechanism of pathogenesis has not been clarified due to the small total number of patients. We herein report on our experience with two cases of familial achalasia in which the involvement of genetic inheri...

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Bibliographic Details
Published in:Surg Case Rep
Main Authors: Hoshino, Masato, Omura, Nobuo, Yano, Fumiaki, Yamamoto, Se Ryung, Matsuda, Minoru, Yanaga, Katsuhiko
Format: Artigo
Language:Inglês
Published: Springer Berlin Heidelberg 2017
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Case Report
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC5422213/
https://ncbi.nlm.nih.gov/pubmed/28485000
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40792-017-0340-0
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