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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Detalhes bibliográficos
Publicado no:BMC Gastroenterol
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2020
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7268223/
https://ncbi.nlm.nih.gov/pubmed/32487124
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12876-020-01238-7
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