Evidence map›Paper›PMID 36542593›Full record

ArticleRevista de la Facultad de Ciencias Medicas (Cordoba, Argentina)2022

[Massive aortic regurgitation with giant aorta aneurysm in Marfan syndrome]

Juan Pablo Ricarte-Bratti, Layla Florencia Martínez, Julio Oscar Emilio Bono, Ignacio Córdoba, Roque Augusto Córdoba

Abstract readEnglish Abstract
In one paragraph

Article in Revista de la Facultad de Ciencias Medicas (Cordoba, Argentina), 2022. 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.

Juan Pablo Ricarte-BrattiSanatorio Allende. jpricartebratti@gmail.com.
Layla Florencia MartínezSanatorio Allende. lflorenciamartinez21@gmail.com.
Julio Oscar Emilio BonoSanatorio Allende. jbonomd@sanatorioallende.com.
Ignacio CórdobaSanatorio Allende. cordobaigna@hotmail.com.
Roque Augusto CórdobaSanatorio Allende. roquecordoba@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Marfan syndrome is an autosomal dominant hereditary disease that compromises various systems that usually require a multidisciplinary approach. The cause of Marfan syndrome is unknown, but recent genetic studies have related this disease to an extracellular microfibrillar defect located on chromosome 15q15-q21.3. Due to the severity of the signs and symptoms the diagnosis is usually at a very young age. We report a patient with extreme Marfan syndrome with all the particulars that this syndrome offers.

Indexed as

Aortic AneurysmAortic Valve InsufficiencyMarfan SyndromeAortaHumansaortic aneurysmaortic regurgitation.Marfan syndrome

Identifiers

PMID36542593
PMCPMC9987305

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.