Evidence map›Paper›PMID 38488524›Full record

ArticleGenetics and molecular biology2024

Disease progression in Sanfilippo type B: Case series of Brazilian patients.

Yorran Hardman Araújo Montenegro, Francyne Kubaski, Franciele Barbosa Trapp, Mariluce Riegel-Giugliani, Carolina Fischinger Moura de Souza, Erlane Marques Ribeiro, Charles Marques Lourenço, Augusto César Cardoso-Dos-Santos, Márcia Gonçalves Ribeiro, Chong Ae Kim and 7 more

Open access · goldAbstract read
In one paragraph

Article in Genetics and molecular biology, 2024. 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
1.0field-weighted citation impact, top 26% 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, 3 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

17 authors at 9 institutions in 2 countries.

Yorran Hardman Araújo MontenegroHospital de Clínicas de Porto Alegre, Serviço de Genética Médica, Porto Alegre, RS, Brazil.ORCID http://orcid.org/0000-0002-0684-1818
Francyne KubaskiHospital de Clínicas de Porto Alegre, Serviço de Genética Médica, Porto Alegre, RS, Brazil.ORCID http://orcid.org/0000-0002-9330-0154
Franciele Barbosa TrappHospital de Clínicas de Porto Alegre, Serviço de Genética Médica, Rede MPS Brasil, Porto Alegre, RS, Brazil.
Mariluce Riegel-GiuglianiCasa dos Raros, Porto Alegre, RS, Brazil.ORCID http://orcid.org/0000-0002-6397-1301
Carolina Fischinger Moura de SouzaHospital de Clínicas de Porto Alegre, Serviço de Genética Médica, Porto Alegre, RS, Brazil.ORCID http://orcid.org/0000-0002-7280-6260
Erlane Marques RibeiroHospital Infantil Albert Sabin, Serviço de Genética Médica, Fortaleza, CE, Brazil.ORCID http://orcid.org/0000-0002-7104-0128
Charles Marques LourençoCentro Universitário Estácio, Ribeirão Preto, SP, Brazil.
Augusto César Cardoso-Dos-SantosHospital Infantil Albert Sabin, Serviço de Genética Médica, Fortaleza, CE, Brazil.ORCID http://orcid.org/0000-0002-1499-9105
Márcia Gonçalves RibeiroUniversidade Federal do Rio de Janeiro, Instituto de Puericultura e Pediatria Martagão Gesteira, Serviço de Genética Médica, Rio de Janeiro, RJ, Brazil.ORCID http://orcid.org/0000-0001-8906-0189
Chong Ae KimUniversidade de São Paulo, Faculdade de Medicina, Hospital das Clínicas, Instituto da Criança, São Paulo, SP, Brazil.
Matheus Augusto Araújo CastroUniversidade de São Paulo, Faculdade de Medicina, Hospital das Clínicas, Instituto da Criança, São Paulo, SP, Brazil.
Emília Katiane EmbiruçuUniversidade Federal da Bahia, Complexo Hospitalar Universitário Professor Edgar Santos, Departamento de Ciências da Vida, Salvador, BA, Brazil.
Carlos Eduardo SteinerUniversidade Estadual de Campinas, Faculdade de Ciências Médicas, Departamento de Medicina Translacional, São Paulo, SP, Brazil.ORCID http://orcid.org/0000-0001-5148-3063
Filippo Pinto E VairoMayo Clinic, Center for Individualized Medicine, Rochester, MN, USA.ORCID http://orcid.org/0000-0001-6030-1903
Guilherme BaldoHospital de Clínicas de Porto Alegre, Serviço de Genética Médica, Porto Alegre, RS, Brazil.ORCID http://orcid.org/0000-0003-1598-5861
Roberto GiuglianiHospital de Clínicas de Porto Alegre, Serviço de Genética Médica, Porto Alegre, RS, Brazil.ORCID http://orcid.org/0000-0001-9655-3686
Fabiano de Oliveira PoswarHospital de Clínicas de Porto Alegre, Serviço de Genética Médica, Porto Alegre, RS, Brazil.ORCID http://orcid.org/0000-0002-0804-2876
Hospital de Clínicas de Porto Alegre · BRUniversidade Federal do Rio Grande do Sul · BRHospital Infantil Albert Sabin · BRUniversidade de São Paulo · BREstácio (Brazil) · BRMayo Clinic in Arizona · USUniversidade Estadual de Campinas (UNICAMP) · BRUniversidade Federal da Bahia · BRUniversidade Federal do Rio de Janeiro · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mucopolysaccharidosis type IIIB (MPS IIIB) is caused by deficiency of alpha-N-acetylglucosaminidase, leading to storage of heparan sulphate. The disease is characterized by intellectual disability and hyperactivity, among other neurological and somatic features. Here we studied retrospective data from a total of 19 MPS IIIB patients from Brazil, aiming to evaluate disease progression. Mean age at diagnosis was 7.2 years. Speech delay was one of the first symptoms to be identified, around 2-3 years of age. Behavioral alterations include hyperactivity and aggressiveness, starting around age four. By the end of the first decade, patients lost acquired abilities such as speech and ability to walk. Furthermore, as disease progresses, respiratory, cardiovascular and joint abnormalities were found in more than 50% of the patients, along with organomegaly. Most common cause of death was respiratory problems. The disease progression was characterized in multiple systems, and hopefully these data will help the design of appropriate clinical trials and clinical management guidelines.

Identifiers

PMID38488524
PMCPMC10941728
OpenAlexW4392719359

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.