Evidence map›Paper›PMID 38721552›Full record

ArticleClinical case reports2024

Arterial stroke in a child with Seckel syndrome with a pattern of non-moyamoya vasculopathy.

Samin Alavi, Mitra Khalili, Paniz Mirmoghaddam, Sharareh Kamfar, Negar Shams

Abstract readCase Reports
In one paragraph

Article in Clinical case reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

5 authors.

Samin AlaviPediatric Congenital Hematologic Disorders Research Center Research Institute for Children's Health, Shahid Beheshti University of Medical Sciences Tehran Iran.ORCID https://orcid.org/0000-0001-8118-7329
Mitra KhaliliPediatric Radiology Department Shahid Beheshti University of Medical Sciences Tehran Iran.
Paniz MirmoghaddamPediatric Radiology Department Shahid Beheshti University of Medical Sciences Tehran Iran.
Sharareh KamfarPediatric Congenital Hematologic Disorders Research Center Research Institute for Children's Health, Shahid Beheshti University of Medical Sciences Tehran Iran.
Negar ShamsPediatric Congenital Hematologic Disorders Research Center Research Institute for Children's Health, Shahid Beheshti University of Medical Sciences Tehran Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Seckel syndrome is a rare autosomal recessive disorder, characterized by growth retardation and multiple anomalies associated with CNS vasculopathy. We describe a child with Seckel syndrome who developed a stroke due to non-moyamoya vasculopathy.

Indexed as

CNS vasculopathymicrocephalic primordial dwarfismmoyamoya diseasenon‐moyamoya vessel networkSeckel syndromestroke

Identifiers

PMID38721552
PMCPMC11077224

What OpenQuestion holds

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Registered trials

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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.