Evidence map›Paper›PMID 25009745›Full record

ReviewRadiology research and practice2014

Differential diagnoses of overgrowth syndromes: the most important clinical and radiological disease manifestations.

Letícia da Silva Lacerda, Ursula David Alves, José Fernando Cardona Zanier, Dequitier Carvalho Machado, Gustavo Bittencourt Camilo, Agnaldo José Lopes

Open access · goldAbstract readReview
In one paragraph

Review in Radiology research and practice, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

22 citing papers in PubMed, 41 citations in OpenAlex.

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  12. A neonate with Klippel-Trénaunay syndrome: a case report.Journal of medical case reports · 2021
    Article
  13. Chiari I malformation with Klippel-Trenaunay syndrome: case report and review of the literature.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2021
    Review
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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

6 authors at 1 institution in 1 country.

Letícia da Silva LacerdaDepartment of Radiology, State University of Rio de Janeiro, 20551-030 Rio de Janeiro, RJ, Brazil.
Ursula David AlvesDepartment of Radiology, State University of Rio de Janeiro, 20551-030 Rio de Janeiro, RJ, Brazil.
José Fernando Cardona ZanierDepartment of Radiology, State University of Rio de Janeiro, 20551-030 Rio de Janeiro, RJ, Brazil.
Dequitier Carvalho MachadoDepartment of Radiology, State University of Rio de Janeiro, 20551-030 Rio de Janeiro, RJ, Brazil ; Postgraduate Programme in Medical Sciences, State University of Rio de Janeiro, 20550-170 Rio de Janeiro, RJ, Brazil.
Gustavo Bittencourt CamiloDepartment of Radiology, State University of Rio de Janeiro, 20551-030 Rio de Janeiro, RJ, Brazil ; Postgraduate Programme in Medical Sciences, State University of Rio de Janeiro, 20550-170 Rio de Janeiro, RJ, Brazil.
Agnaldo José LopesPostgraduate Programme in Medical Sciences, State University of Rio de Janeiro, 20550-170 Rio de Janeiro, RJ, Brazil.
Universidade do Estado do Rio de Janeiro · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Overgrowth syndromes comprise a heterogeneous group of diseases that are characterized by excessive tissue development. Some of these syndromes may be associated with dysfunction in the receptor tyrosine kinase (RTK)/PI3K/AKT pathway, which results in an increased expression of the insulin receptor. In the current review, four overgrowth syndromes were characterized (Proteus syndrome, Klippel-Trenaunay-Weber syndrome, Madelung's disease, and neurofibromatosis type I) and illustrated using cases from our institution. Because these syndromes have overlapping clinical manifestations and have no established genetic tests for their diagnosis, radiological methods are important contributors to the diagnosis of many of these syndromes. The correlation of genetic discoveries and molecular pathways that may contribute to the phenotypic expression is also of interest, as this may lead to potential therapeutic interventions.

Identifiers

PMID25009745
PMCPMC4070411
OpenAlexW2132647355

What OpenQuestion holds

Textmetadata
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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.