ArticleFrontiers in pediatrics2025
Clinical characteristics and gene analysis of long QT syndrome in 15 children.
Article in Frontiers in pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Objective: To elucidate the genetic and clinical characteristics of children diagnosed with long QT syndrome (LQTS) at our institution. Study design: This was a retrospective study. Clinical data and gene detection results of 15 cases diagnosed with congenital LQTS at our center from January 1, 2018 to December 30, 2023 were collected and analyzed using independent sample Results: The 15 LQTS cases included 7 females and 8 males. The mean age of onset for females (11.83 ± 3.48 years) was later than that for males (8.06 ± 2.50 years), and the mean QTc value for females (564.57 ± 20.72 ms) was higher than that for males (502. 25 ± 48.62 ms), both differences were statistically significant ( Conclusions: In this cohort, age of onset and QTc value are different between male and female. The most common primary symptom of LQTS is syncope. Most LQTS patients have a mutated gene inherited from their parents, and the most common pathogenic gene is
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.