Evidence map›Paper›PMID 32185055›Full record

ArticleClinical case reports2020

Cardiofaciocutaneous syndrome with rare structural variant in

Domenico Dell'Edera, Lucantonio Debellis, Angela Mitidieri, Annunziata Anna Epifania, Eustachio Cuscianna, Arianna Allegretti

Open access · goldAbstract readCase Reports
In one paragraph

Article in Clinical case reports, 2020. 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
0.2field-weighted citation impact, top 51% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  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

6 authors at 1 institution in 1 country.

Domenico Dell'EderaUnit of Cytogenetic and Molecular Genetics "Madonna delle Grazie" Hospital Matera Italy.ORCID https://orcid.org/0000-0002-0604-5512
Lucantonio DebellisUnit of Cytogenetic and Molecular Genetics "Madonna delle Grazie" Hospital Matera Italy.
Angela MitidieriUnit of Cytogenetic and Molecular Genetics "Madonna delle Grazie" Hospital Matera Italy.
Annunziata Anna EpifaniaUnit of Cytogenetic and Molecular Genetics "Madonna delle Grazie" Hospital Matera Italy.
Eustachio CusciannaUnit of Cytogenetic and Molecular Genetics "Madonna delle Grazie" Hospital Matera Italy.
Arianna AllegrettiUnit of Cytogenetic and Molecular Genetics "Madonna delle Grazie" Hospital Matera Italy.
Ospedale Madonna Delle Grazie · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We describe a girl with clinical signs of cardiofaciocutaneous syndrome who simultaneously presents a mutation in the BRAF gene and a 9p24.3 microduplication. This genetic condition has never been described in the literature and could explain the phenotypic variability observed in the girl.

Indexed as

BRAFcardiofaciocutaneous syndromeDOCK8multiple congenital anomalyneurodevelopmental disorders

Identifiers

PMID32185055
PMCPMC7069886
OpenAlexW3006619279

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.