Evidence map›Paper›PMID 39913066›Full record

ArticleJournal of community genetics2025

Redefining the approach to rare diseases: the experience of "Casa dos Raros" in Brazil.

Roberto Giugliani, Bibiana Mello de Oliveira, Bruna Baierle Guaraná, Tássia Tonon, Franciele Barbosa Trapp, Fernando Machado da Costa, Larissa Pozzebon da Silva, Guilherme Baldo, Mariluce Riegel-Giugliani, Fabrizio Barbosa and 2 more

Abstract read
In one paragraph

Article in Journal of community genetics, 2025. 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
–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

2 citing papers in PubMed.

  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

12 authors.

Roberto GiuglianiCasa dos Raros, Rua São Manoel, 730, 90610-261, Porto Alegre, RS, Brazil.ORCID http://orcid.org/0000-0001-9655-3686
Bibiana Mello de OliveiraCasa dos Raros, Rua São Manoel, 730, 90610-261, Porto Alegre, RS, Brazil. bibiana.oliveira@cdr.org.br.ORCID http://orcid.org/0000-0002-2679-6858
Bruna Baierle GuaranáCasa dos Raros, Rua São Manoel, 730, 90610-261, Porto Alegre, RS, Brazil.ORCID http://orcid.org/0000-0003-3139-8173
Tássia TononCasa dos Raros, Rua São Manoel, 730, 90610-261, Porto Alegre, RS, Brazil.
Franciele Barbosa TrappCasa dos Raros, Rua São Manoel, 730, 90610-261, Porto Alegre, RS, Brazil.
Fernando Machado da CostaCasa dos Raros, Rua São Manoel, 730, 90610-261, Porto Alegre, RS, Brazil.
Larissa Pozzebon da SilvaCasa dos Raros, Rua São Manoel, 730, 90610-261, Porto Alegre, RS, Brazil.
Guilherme BaldoCasa dos Raros, Rua São Manoel, 730, 90610-261, Porto Alegre, RS, Brazil.
Mariluce Riegel-GiuglianiCasa dos Raros, Rua São Manoel, 730, 90610-261, Porto Alegre, RS, Brazil.
Fabrizio BarbosaCasa dos Raros, Rua São Manoel, 730, 90610-261, Porto Alegre, RS, Brazil.
Antoine DaherCasa dos Raros, Rua São Manoel, 730, 90610-261, Porto Alegre, RS, Brazil.
Carolina Fischinger Moura de SouzaCasa dos Raros, Rua São Manoel, 730, 90610-261, Porto Alegre, RS, Brazil.ORCID http://orcid.org/0000-0002-7280-6260

Funding

Casa Hunter, São Paulo, Brazil N/AInstituto Genética para Todos, Porto Alegre, Brazil N/A
6 · The paper itself

Abstract

Rare diseases include 6,000-8,000 different conditions, over 70% of them having a genetic cause. Most cases have early manifestations (in childhood and adolescence), and just a small fraction (around 5%) has specific therapies available. Nevertheless, appropriate management measures contribute to improve the quality of life of patients and families. They affect up to 3.5-5.9% of the world's population and are recently attracting attention from international agencies such as the United Nations and the World Health Organization. In Brazil, a condition is considered rare when there are no more than 65 people affected in each 100,000 inhabitants and it is estimated that around 12 million people in the country may present one of these conditions, which represents a significant burden to the family and to the health care system. Despite concrete advances observed in the last decades, there are still significant unmet needs for persons living with rare diseases in Brazil. With the main aim of shortening the journey of patients with rare diseases in Brazil, we envisioned a model that involves comprehensive clinical and laboratorial multiprofessional evaluations, with intensive use of telemedicine and genomics. The model includes a strong activity in education, training and research, and has several parallel initiatives (biobank, registry, undiagnosed disease program, information services, extramural diagnostic support), in addition to strategic partnerships, that make the overall project stronger. This report describes the system in place at the pilot unit of Casa dos Raros (that started activities in 2023, in Porto Alegre, Brazil) and the stimulating preliminary results, which indicate a significant reduction in the diagnostic journey. This model, that operates as a charity and does not charge any fees to patients and families, will be replicated in other regions of Brazil, with the opening of a second unit planned to occur in the near future in Sao Paulo.

Indexed as

BrazilCasa Dos RarosDiagnostic journeyHealth systemsInnovation in healthMultidisciplinary approachRare diseasesTelemedicine

Identifiers

PMID39913066
PMCPMC12321710

What OpenQuestion holds

Textmetadata
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.