Evidence map›Paper›PMID 39086440›Full record

ArticleJournal of pediatric genetics2024

Novel

R Ramos-Mejía, M Del Pino, M Aza-Carmona, S Abbate, M G Obregon, K E Heath, V Fano

Abstract read
In one paragraph

Article in Journal of pediatric genetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–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

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Filamin B (Genes · 2026
    Pooled it
  2. Article
  3. Article
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

7 authors.

R Ramos-MejíaGrowth and Development Department, Hospital Garrahan, Buenos Aires, Argentina.ORCID 0000-0003-1717-2805
M Del PinoGrowth and Development Department, Hospital Garrahan, Buenos Aires, Argentina.ORCID 0000-0001-6095-7080
M Aza-CarmonaCentro de Investigacion Biomédica en Red Enfermedades Raras (CIBERER), ISCIII, Madrid, España.ORCID 0000-0003-4448-9541
S AbbateGenetics Department, Hospital Garrahan, Buenos Aires, Argentina.ORCID 0000-0002-4859-3787
M G ObregonGenetics Department, Hospital Garrahan, Buenos Aires, Argentina.ORCID 0000-0001-7129-8009
K E HeathCentro de Investigacion Biomédica en Red Enfermedades Raras (CIBERER), ISCIII, Madrid, España.ORCID 0000-0002-5816-7044
V FanoGrowth and Development Department, Hospital Garrahan, Buenos Aires, Argentina.ORCID 0000-0003-3311-2220

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spondylocarpotarsal synostosis syndrome (SCT) is a very rare skeletal dysplasia characterized by vertebral, carpal, and tarsal fusion; growth retardation; and mild dysmorphic facial features. Variants in

Indexed as

carpal coalitionfilamin Bscoliosisskeletal dysplasiaspondylocarpotarsal synostosis syndrome

Identifiers

PMID39086440
PMCPMC11288708

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.