Evidence map›Paper›PMID 35212703›Full record

ArticleJornal brasileiro de nefrologia

Brazilian consensus recommendations for the diagnosis, screening, and treatment of individuals with fabry disease: Committee for Rare Diseases - Brazilian Society of Nephrology/2021.

Cassiano Augusto Braga Silva, Luis Gustavo Modelli de Andrade, Maria Helena Vaisbich, Fellype de Carvalho Barreto

Open access · diamondAbstract readConsensus Statement
In one paragraph

Article in Jornal brasileiro de nefrologia. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Fabry Disease and Its Different Phenotypes.Arquivos brasileiros de cardiologia · 2025
    Article
  6. Article
  7. Observational
  8. Review
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

4 authors at 4 institutions in 2 countries.

Cassiano Augusto Braga SilvaClínica de Nefrologia Senhor do Bonfim, Feira de Santana, BA, Brasil.ORCID http://orcid.org/0000-0002-7126-5028
Luis Gustavo Modelli de AndradeUniversidade Estadual Paulista, Botucatu, SP, Brasil.ORCID http://orcid.org/0000-0002-0230-0766
Maria Helena VaisbichUniversidade de São Paulo, São Paulo, SP, Brasil.ORCID http://orcid.org/0000-0002-6084-7831
Fellype de Carvalho BarretoUniversidade Federal do Paraná, Curitiba, PR, Brasil.ORCID http://orcid.org/0000-0002-6394-9227
Sociedad Española de Nefrología · ESUniversidade de São Paulo · BRUniversidade Estadual Paulista (Unesp) · BRUniversidade Federal do Paraná · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fabry disease (FD) is an X-linked inherited disorder caused by mutations in the GLA gene encoding enzyme alpha-galactosidase A (α-Gal A). The purpose of this study was to produce a consensus statement to standardize the recommendations concerning kidney involvement in FD and provide advice on the diagnosis, screening, and treatment of adult and pediatric patients. This consensus document was organized from an initiative led by the Committee for Rare Diseases (Comdora) of the Brazilian Society of Nephrology (SBN). The review considered randomized clinical trials, real-world data studies, and the expertise of its authors. The purpose of this consensus statement is to help manage patient and physician expectations concerning the outcomes of treatment. Our recommendations must be interpreted within the context of available evidence. The decisions pertaining to each individual case must be made with the involvement of patients and their families and take into account not only the potential cost of treatment, but also concurrent conditions and personal preferences. The Comdora intends to update these recommendations regularly so as to reflect recent literature evidence, real-world data, and appreciate the professional experience of those involved. This consensus document establishes clear criteria for the diagnosis of FD and for when to start or stop specific therapies or adjuvant measures, to thus advise the medical community and standardize clinical practice.

Indexed as

Fabry DiseaseNephrologyAdultalpha-GalactosidaseBrazilChildHumansRare Diseasesalpha-Galactosidase

Identifiers

PMID35212703
PMCPMC9269181
OpenAlexW4214521169

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.