Evidence map›Paper›PMID 40842752›Full record

ArticleCureus2025

A Rare Case of Congenital Knee Dislocation.

Mohammed M Mumtaz, Molly R Posa, Elahe M Shychuk

Abstract readCase Reports
In one paragraph

Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Mohammed M MumtazPediatrics, University of Florida College of Medicine, Gainesville, USA.
Molly R PosaPediatrics, University of Florida College of Medicine, Gainesville, USA.
Elahe M ShychukPediatrics, University of Florida College of Medicine, Gainesville, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Congenital knee dislocation (CKD) is a rare condition that can present as an isolated finding or in association with genetic syndromes. It is most commonly diagnosed postnatally and classified into three grades based on severity. While generally having a favorable prognosis, particularly for milder cases, prompt treatment is crucial. We present a case of CKD successfully treated with conservative measures, with serial casting and Pavlik harness, in an otherwise healthy infant. This report aims to increase awareness of the clinical presentation and management of CKD in general practitioners given its rarity.

Indexed as

congenital dislocation of the kneecongenital hip dislocationcongenital orthopedic abnormalitiesdevelopmental dysplasia of the hipneonatal orthopedic abnormalitiespackaging disorderspavlik harness

Identifiers

PMID40842752
PMCPMC12367285

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

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.