17q12 Knowledge Basedeletion syndrome · static snapshot
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Source updated Genes & inheritance 1 supporting source confidence 80% novelty 80%

Updated: A familial case report of 17q12 recurrent deletion syndrome: clinical and molecular characterization.

pubmed changed: +2/-13 sentences since the previous capture.

More source updated

How this was derived

Version 2 captured 2026-11-14. Newly added text includes: “A familial case report of 17q12 recurrent deletion syndrome: clinical and molecular characterization. This article presents the first reported familial case of 17q12 recurrent deletion syndrome in Russia, involving a female patient with diabetes and her daughter diagnosed with atypical autism without intellectual disability.”

Generated 2026-11-14, last changed today. Dedup key update:15. 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)

A familial case report of 17q12 recurrent deletion syndrome: clinical and molecular characterization. peer_reviewed · published 2026-11-14T00:53:16+00:00 · live page
A familial case report of 17q12 recurrent deletion syndrome: clinical and molecular characterization. This article presents the first reported familial case of 17q12 recurrent deletion syndrome in Russia, involving a female patient with diabetes and her daughter diagnosed with atypical autism without intellectual disability.

Supporting documents (1)

DocumentSourcePublishedSeenRelevance
A familial case report of 17q12 recurrent deletion syndrome: clinic... pubmed 2026-01-01 yesterday 1.00