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A retrospective analysis of prenatal genetic results in fetal hydronephrosis

Objective To discuss the application value of technologies such as chromosome microarray analysis (CMA) in fetuses with hydronephrosis and pyelectasis.

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How this was derived

Indexed from **pmc** on 2026-11-13 (relevance 1.00, tier peer_reviewed).

Generated 2026-11-13, last changed yesterday. Dedup key newdoc:369. 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 retrospective analysis of prenatal genetic results in fetal hydronephrosis peer_reviewed · published 2025-01-01 · live page
Comparison of fetal anomaly detection rates with CMA in moderate to severe hydronephrosis groups versus mild hydronephrosis groups In 83 specimens, divided into two groups based on the severity of hydronephrosis, the detection rate of fetuses carrying variants by CMA in the moderate-to-severe hydronephrosis group was 10%, while in the mild hydronephrosis group it was 37.21%.

Supporting documents (1)

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A retrospective analysis of prenatal genetic results in fetal hydro... pmc 2025-01-01 yesterday 1.00