Evidence map›Paper›PMID 25054766›Full record

ArticleAnais brasileiros de dermatologia

Syndrome in question.

Sheila Itamara Ferreira do Couto Meireles, Sônia Maria Fonseca de Andrade, Maria Fernanda Gomes, Fernanda Aalmeida Nunes Castro, Antonio José Tebcherani

Abstract readCase Reports
In one paragraph

Article in Anais brasileiros de dermatologia. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Sheila Itamara Ferreira do Couto MeirelesComplexo Hospitalar Padre Bento de Guarulhos, Guarulhos, SP, Brazil.
Sônia Maria Fonseca de AndradeComplexo Hospitalar Padre Bento de Guarulhos, Guarulhos, SP, Brazil.
Maria Fernanda GomesComplexo Hospitalar Padre Bento de Guarulhos, Guarulhos, SP, Brazil.
Fernanda Aalmeida Nunes CastroComplexo Hospitalar Padre Bento de Guarulhos, Guarulhos, SP, Brazil.
Antonio José TebcheraniComplexo Hospitalar Padre Bento de Guarulhos, Guarulhos, SP, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rendu-Osler-Weber Syndrome also known as Hereditary Hemorrhagic Telangiectasia is a rare systemic fibrovascular dysplasia, with dominant autosomal inheritance. It is characterized by recurrent epistaxis, mucocutaneous telangiectasia, visceral arteriovenous malformation and positive family history. There may be hematologic, neurologic, dermatologic and gastrointestinal complications. Therapy is supportive and aimed at preventing complications. In this article we report a case of Rendu-Osler-Weber in a 64 year-old man, with history of mucocutaneous telangiectasia since the third decade of life, recurrent epistaxis, positive family history and vascular ectasia in the gastrointestinal tract.

Indexed as

Endothelial CellsHumansMaleMiddle AgedSyndromeTelangiectasia, Hereditary HemorrhagicTongue Diseases

Identifiers

PMID25054766
PMCPMC4148293

What OpenQuestion holds

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LicenceCC BY-NC
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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.