17q12, explained for kidsdeletion syndrome · static snapshot
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17q12 deletion syndrome presenting with chronic pancreatitis: a case report

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

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How this was derived

Indexed from **openalex** on 2026-11-13 (relevance 1.00, tier peer_reviewed).

Generated 2026-11-13, last changed yesterday. Dedup key newdoc:526. 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 2026-04-15 · live page
We report an 18-year-old female with recurrent upper abdominal pain, steatorrhea, and dyspepsia.

Supporting documents (1)

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17q12 deletion syndrome presenting with chronic pancreatitis: a case report openalex 2026-04-15 yesterday 1.00