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

Updated: Atypical presentation of HNF1β gene mutation mimicking type 2 diabetes: Case report and literature review

pmc changed: +4/-28 sentences since the previous capture.

More source updated

How this was derived

Version 2 captured 2026-11-14. Newly added text includes: “Hepatocyte nuclear factor 1β ( HNF1β )-related disease is a rare autosomal dominant genetic disorder. Hepatocyte nuclear factor 1β ( HNF1β )-related disease is a rare autosomal dominant genetic disorder. We would like to thank the patient and his family members for their contribution to this study.”

Generated 2026-11-14, last changed today. Dedup key update:241. 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)

Atypical presentation of HNF1β gene mutation mimicking type 2 diabetes: Case report and literature review peer_reviewed · published 2026-11-14T01:36:54+00:00 · live page
Hepatocyte nuclear factor 1β ( HNF1β )-related disease is a rare autosomal dominant genetic disorder. Hepatocyte nuclear factor 1β ( HNF1β )-related disease is a rare autosomal dominant genetic disorder. We would like to thank the patient and his family members for their contribution to this study.

Supporting documents (1)

DocumentSourcePublishedSeenRelevance
Atypical presentation of HNF1β gene mutation mimicking type 2 diabe... pmc 2025-01-01 yesterday 1.00