Evidence map›Paper›PMID 42176704›Full record

ArticleJornal de pediatria

Brazilian growth charts for 22q11.2 deletion syndrome from birth to 17 years.

Amanda de Sousa Lima Strafacci, Fabio Bertapelli, Bruna Fagundes Rodrigues Alaite, Júlia Lôndero Heleno, Débora Gusmão Melo, Maria Isabel Riesemberg, Carolina de Souza Araújo, Fernanda Araújo Romera, Ana Carolina Xavier, Stela Carpini Dantas and 3 more

Abstract readMulticenter Study
In one paragraph

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

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0citing papers in PubMed
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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

13 authors.

Amanda de Sousa Lima StrafacciUniversidade Estadual de Campinas (UNICAMP), Faculdade de Ciências Médicas (FCM), Departamento de Pediatria, Campinas, SP, Brazil.
Fabio BertapelliUniversidade Federal de São Paulo (UNIFESP), Departamento de Ciências do Movimento Humano, Santos, SP, Brazil.
Bruna Fagundes Rodrigues AlaiteUniversidade Estadual de Campinas (UNICAMP), Faculdade de Ciências Médicas (FCM), Departamento de Medicina Translacional, Campinas, SP, Brazil.
Júlia Lôndero HelenoUniversidade Estadual de Campinas (UNICAMP), Faculdade de Ciências Médicas (FCM), Departamento de Medicina Translacional, Campinas, SP, Brazil.
Débora Gusmão MeloUniversidade Federal de São Paulo (UNIFESP), Escola Paulista de Medicina, Departamento de Morfologia e Genética, Divisão de Genética, São Paulo, SP, Brazil.
Maria Isabel RiesembergUniversidade Federal de São Paulo (UNIFESP), Escola Paulista de Medicina, Departamento de Morfologia e Genética, Divisão de Genética, São Paulo, SP, Brazil.
Carolina de Souza AraújoUniversidade Federal de São Paulo (UNIFESP), Escola Paulista de Medicina, Departamento de Morfologia e Genética, Divisão de Genética, São Paulo, SP, Brazil.
Fernanda Araújo RomeraUniversidade Federal de São Paulo (UNIFESP), Escola Paulista de Medicina, Departamento de Morfologia e Genética, Divisão de Genética, São Paulo, SP, Brazil.
Ana Carolina XavierCentro de Tratamento e Reabilitação de Fissuras Labiopalatinas, Centrinho Prefeito Luiz Gomes, Joinville, SC, Brazil.
Stela Carpini DantasUniversidade Estadual de Campinas (UNICAMP), Faculdade de Ciências Médicas (FCM), Centro de Pesquisa em Pediatria (CIPED), Laboratório de Crescimento e Desenvolvimento (LabCreD), Campinas, SP, Brazil.
Gil Guerra-JuniorUniversidade Estadual de Campinas (UNICAMP), Faculdade de Ciências Médicas (FCM), Departamento de Pediatria, Campinas, SP, Brazil; Universidade Estadual de Campinas (UNICAMP), Faculdade de Ciências Médicas (FCM), Centro de Pesquisa em Pediatria (CIPED), Laboratório de Crescimento e Desenvolvimento (LabCreD), Campinas, SP, Brazil. Electronic address: gilguer@unicamp.br.
Vera Lúcia Gil-da-Silva-LopesUniversidade Estadual de Campinas (UNICAMP), Departamento de Genética Médica e Medicina Genômica, Campinas, SP, Brazil.
SD22q11.2 Research Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo develop Brazilian growth charts for weight, height, body mass index (BMI), and head circumference (HC), stratified by sex, for patients with 22q11.2 deletion syndrome (22q11.2DS) from birth to 17 years.

methodsThis multicenter, retrospective, longitudinal study included 1826 anthropometric data collected through medical record review of 113 patients with a laboratory-confirmed diagnosis of 22q11.2DS who were followed at 11 centers participating in the Craniofacial Brazil Project. The 3rd, 10th, 25th, 50th, 75th, 90th, and 97th percentiles for anthropometric parameters were developed for males and females from birth to 17 years old using the Lambda-Mu-Sigma (LMS) method and graphically compared with reference percentiles from the Centers for Disease Control and Prevention using the Tidyverse package in R software.

resultsA growth pattern distinct from that of the reference population was observed, with more pronounced deficits in height and weight during the first two years of life in both sexes. After this period, partial recovery in height was observed, more evident in females, whereas the deficit remained more pronounced in males. Differences in BMI and HC were less marked.

conclusionThe Brazilian growth charts for 22q11.2DS provide more appropriate parameters for clinical monitoring and individualized care of this population.

Indexed as

DiGeorge SyndromeGrowth ChartsAdolescentBody HeightBody Mass IndexBody WeightBrazilChildChild, PreschoolFemaleHeadHumansInfantInfant, NewbornLongitudinal StudiesMale22q11.2 deletion syndromeBody heightBody mass indexBody weightDiGeorge syndromeGrowth charts

Identifiers

PMID42176704
PMCPMC13241978

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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.