17q12 Knowledge Basedeletion syndrome · static snapshot
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Frequency / statistic kidney and urinary tract 1 supporting source confidence 97% novelty 60%

While up to 50% of children requiring kidney replacement therapy have congenital anomalies of the kidney and urinary tra

A source reports “50%” in the context of kidney: “While up to 50% of children requiring kidney replacement therapy have congenital anomalies of the kidney and urinary tract (CAKUT), they represent only a fraction of the total patient population with CAKUT.”

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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:50%. 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 (4 quotes)

A Case of Amyotrophic Lateral Sclerosis With Coexisting Maturity-onset Diabetes of the Young Type 5. peer_reviewed · published 2025-11-01 · live page
IGF-1 has a 50% sequence homology with insulin and is able to elicit nearly the same hypoglycemic effects [ 55 ].
17q12 Recurrent Deletion Syndrome in Childhood peer_reviewed · published 2025-01-01 · live page
MODY5 occurs in approximately 30-50% of deletion carriers, although the onset is typically in adolescence or early adulthood.
Familial Multicystic Dysplastic Kidney Associated with HNF1B Mutation: A Sibling Case Report peer_reviewed · published 2026-10-12 · live page
Renal cysts (50%) and multicystic dysplastic kidney (MCDK) (37.5%) are the most common renal phenotypes.
Translational strategies to uncover the etiology of congenital anomalies of the kidney and urinary tract peer_reviewed · published 2024-01-01 · live page
While up to 50% of children requiring kidney replacement therapy have congenital anomalies of the kidney and urinary tract (CAKUT), they represent only a fraction of the total patient population with CAKUT.

Supporting documents (4)

ArticleSourcePublishedSeenRelevance
A Case of Amyotrophic Lateral Sclerosis With Coexisting Maturity-on... pubmed 2025-11-01 yesterday 1.00
17q12 Recurrent Deletion Syndrome in Childhood pmc 2025-01-01 yesterday 1.00
Familial Multicystic Dysplastic Kidney Associated with HNF1B Mutati... openalex 2026-10-12 yesterday 1.00
Translational strategies to uncover the etiology of congenital anom... pmc 2024-01-01 yesterday 1.00