17q12 Knowledge Basedeletion syndrome · static snapshot
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Source updated kidney and urinary tract 1 supporting source confidence 80% novelty 80%

Updated: 17q12 deletion syndrome presenting with chronic pancreatitis: a case report.

pubmed changed: +2/-8 sentences since the previous capture.

How this was derived

Version 2 captured 2026-11-14. Newly added text includes: “17q12 deletion syndrome presenting with chronic pancreatitis: a case report. 17q12 deletion syndrome is a rare autosomal dominant disorder classically characterized by renal cystic disease, maturity-onset diabetes of the young type 5 (MODY5), and Müllerian duct anomalies (e. g., MRKH syndrome).”

Generated 2026-11-14, last changed today. Dedup key update:17. The engine re-checks this insight on every analysis run; if more sources agree, its corroboration and confidence go up and it reappears as “new”.

Evidence (1 quote)

17q12 deletion syndrome presenting with chronic pancreatitis: a case report. peer_reviewed · published 2026-11-14T00:53:36+00:00 · live page
17q12 deletion syndrome presenting with chronic pancreatitis: a case report. 17q12 deletion syndrome is a rare autosomal dominant disorder classically characterized by renal cystic disease, maturity-onset diabetes of the young type 5 (MODY5), and Müllerian duct anomalies (e. g., MRKH syndrome).

Supporting documents (1)

DocumentSourcePublishedSeenRelevance
17q12 deletion syndrome presenting with chronic pancreatitis: a cas... pubmed 2026-01-01 yesterday 1.00