Evidence map›Paper›PMID 37283908›Full record

ArticleJournal of cardiology cases2023

Early-onset Marfan syndrome with a novel missense mutation: A case report.

Kana Soma, Yosuke Kitagawa, Tsutomu Toki, Fumitake Miura, Jun Shimada, Tomohiko Sato, Ko Kudo, Katsuki Otani, Toru Takahashi, Kiminori Terui

Open access · bronzeAbstract readCase Reports
In one paragraph

Article in Journal of cardiology cases, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 97% of its field
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

1 citing paper in PubMed, 0 citations in OpenAlex.

  1. Genetic Variants in Recurrent Euploid Pregnancy Loss.medRxiv : the preprint server for health sciences · 2025
    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

10 authors at 1 institution in 1 country.

Kana SomaDepartment of Pediatrics, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
Yosuke KitagawaDepartment of Pediatrics, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
Tsutomu TokiDepartment of Pediatrics, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
Fumitake MiuraDepartment of Pediatrics, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
Jun ShimadaDepartment of Pediatrics, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
Tomohiko SatoDepartment of Pediatrics, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
Ko KudoDepartment of Pediatrics, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
Katsuki OtaniDepartment of Pediatrics, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
Toru TakahashiDepartment of Pediatrics, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
Kiminori TeruiDepartment of Pediatrics, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
Hirosaki University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Early-onset Marfan syndrome (eoMFS) progresses rapidly, starting during the neonatal period, causes severe clinical disease, and has a poor prognosis. The genetic abnormality associated with eoMFS is located in a so-called critical neonatal region in exons 25-26 of the Learning objective: We identified a novel missense mutation located in exons 25-26 of the Fibrillin-1 gene in a neonate with early-onset Marfan syndrome (eoMFS) who died of severe early heart failure shortly after birth. This mutation was located in a narrowly defined critical neonatal region, recently reported to cause eoMFS, and its clinical profile was consistent with early-onset severe heart failure. In addition to ultrasonography, genetic analysis of this region is important for predicting prognosis in eoMFS.

Indexed as

Aortic root dilatationArachnodactylyEarly-onset Marfan syndromeFBN1 geneMissense variantNext-generation sequencing

Identifiers

PMID37283908
PMCPMC10240411
OpenAlexW4323823267

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.