17q12, explained for kidsdeletion syndrome · static snapshot
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A number from a study Learning, talking and behaviour 1 supporting source confidence 97% novelty 60%

The features observed in patients with recurrent and large overlapping duplications also significantly complement the kn

A source reports “3%” in the context of neurodevelopment: “The features observed in patients with recurrent and large overlapping duplications also significantly complement the known symptoms; musculoskeletal, brain, and heart anomalies, as well as epilepsy and sleep disorders, which occur with a frequency of 3%-31%, ”

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Generated 2026-11-13, last changed yesterday. Dedup key freq:3%. 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 (2 quotes)

Clinical characteristics and etiologies of hypomagnesemia in children: a single-center retrospective cohort study peer_reviewed · published 2026-01-01 · live page
2 Proportion of different diseases associated with hypomagnesemia Clinical characteristics We defined renal magnesium wasting as a FEMg greater than 3% or a 24-hour urinary magnesium excretion exceeding 10 mg [ 7 ].
Delineation of the Genetic Architecture and Clinical Polymorphism of 3q29 Duplication Syndrome: A Review of the Literature and a Report of Two Novel Patients With Single‐Gene BDH1 Duplications peer_reviewed · published 2024-01-01 · live page
The features observed in patients with recurrent and large overlapping duplications also significantly complement the known symptoms; musculoskeletal, brain, and heart anomalies, as well as epilepsy and sleep disorders, which occur with a frequency of 3%-31%, are not represented in the Clinical Synopsis.

Supporting documents (2)

StorySourcePublishedSeenRelevance
Clinical characteristics and etiologies of hypomagnesemia in childr... pmc 2026-01-01 yesterday 1.00
Delineation of the Genetic Architecture and Clinical Polymorphism o... pmc 2024-01-01 yesterday 1.00