טוען...
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...
שמור ב:
| הוצא לאור ב: | BMC Gastroenterol |
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| Main Authors: | , , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
BioMed Central
2020
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| נושאים: | |
| גישה מקוונת: | 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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