HIGHLIGHTS
- What: PJS is an uncommon hereditary condition that calls for specialized care and an interdisciplinary approach.
- Who: Ashish Kuruvila and colleagues from the (UNIVERSITY) have published the research work: Review began 07/25/2024 Review ended 07/28/2024 Published 08/01/2024 © Copyright, in the Journal: (JOURNAL) of August/01,/2024
SUMMARY
Dr. Jan Peutz first identified Peutz-Jeghers syndrome (PJS) as a syndrome in 1921. With 64% of cases occurring in the small bowel, stomach, and colon, hamartomatous polyps are most frequently identified in these three organs. Dark blue . . .
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