Juvenile polyposis syndrome might be misdiagnosed as familial adenomatous polyposis: a case report and literature review

BACKGROUND: Juvenile polyposis syndrome (JPS) is a rare disorder characterized by the presence of multiple juvenile polyps in the gastrointestinal tract, and germline mutations in SMAD4 or BMPR1A. Due to its rarity and complex clinical manifestation, misdiagnosis often occurs in clinical practice. C...

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Detalles Bibliográficos
Autores principales: Gao, Xian Hua, Li, Juan, Zhao, Zi Ye, Xu, Xiao Dong, Du, Yi Qi, Yan, Hong Li, Liu, Lian Jie, Bai, Chen Guang, Zhang, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7268223/
https://www.ncbi.nlm.nih.gov/pubmed/32487124
http://dx.doi.org/10.1186/s12876-020-01238-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7268223/
https://www.ncbi.nlm.nih.gov/pubmed/32487124
http://dx.doi.org/10.1186/s12876-020-01238-7

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