17q12 Knowledge Basedeletion syndrome · static snapshot
All content was collected from public internet sources and processed with the help of AI/LLM software. This site is informative only — do not draw conclusions; verify with the original sources. Full disclaimer
Frequency / statistic kidney and urinary tract 1 supporting source confidence 97% novelty 60%

Although individually rare, genetic causes account for end-stage renal disease in 10% to 15% of adults and 70% of childr

A source reports “10%” in the context of kidney: “Although individually rare, genetic causes account for end-stage renal disease in 10% to 15% of adults and 70% of children, and in many of these individuals, genetic testing can identify a specific etiology and meaningfully impact management.”

How this was derived

Numbers are quoted verbatim from the source; check the source before quoting onward.

Generated 2026-11-13, last changed today. Dedup key freq:10%. 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 (3 quotes)

When applied to all-cause chronic kidney disease (CKD) in an adult cohort, a genetic diagnosis is found in ∼10% of patients [ 10 ] (diagnostic yield would likely be higher in paediatric subjects).
Among patients with congenital abnormalities of the kidney and urinary tract, approximately 10% had HNF1B mutations.
Although individually rare, genetic causes account for end-stage renal disease in 10% to 15% of adults and 70% of children, and in many of these individuals, genetic testing can identify a specific etiology and meaningfully impact management.

Supporting documents (3)