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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Bibliographische Detailangaben
Veröffentlicht in:BMC Gastroenterol
Hauptverfasser: 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
Format: Artigo
Sprache:Inglês
Veröffentlicht: BioMed Central 2020
Schlagworte:
Case Report
Online Zugang: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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