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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Detalles Bibliográficos
Autores principales: Hoshino, Masato, Omura, Nobuo, Yano, Fumiaki, Yamamoto, Se Ryung, Matsuda, Minoru, Yanaga, Katsuhiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5422213/
https://www.ncbi.nlm.nih.gov/pubmed/28485000
http://dx.doi.org/10.1186/s40792-017-0340-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5422213/
https://www.ncbi.nlm.nih.gov/pubmed/28485000
http://dx.doi.org/10.1186/s40792-017-0340-0

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