17q12 Knowledge Basedeletion syndrome · static snapshot
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New publication kidney and urinary tract 1 supporting source confidence 97% novelty 75%

Chromosome 17q12 deletion, including HNF1B presenting with recurrent severe cholestasis and profound hypomagnesemia during pregnancy: a case report.

2666-5778 6 2 2026 May AJOG global reports AJOG Glob Rep Chromosome 17q12 deletion, including HNF1B presenting with recurrent severe cholestasis and profound hypomagnesemia during pregnancy: a case report.

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How this was derived

Indexed from **pubmed** on 2026-11-12 (relevance 1.00, tier peer_reviewed).

Generated 2026-11-14, last changed today. Dedup key newdoc:18. 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)

Chromosome 17q12 deletion, including HNF1B presenting with recurrent severe cholestasis and profound hypomagnesemia during pregnancy: a case report. peer_reviewed · published 2026-05-01 · live page
17q12 deletion should be considered in the differential diagnosis when severely elevated bile acids are encountered during pregnancy, particularly in combination with maternal Mullerian anomaly or renal dysfunction, or fetal renal anomaly. © 2026 The Authors.

Supporting documents (1)

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Chromosome 17q12 deletion, including HNF1B presenting with recurren... pubmed 2026-05-01 yesterday 1.00