Pular para o conteúdo
ORPHA:106CID-10 · F84.0DOENÇA RARA
neuro
Também conhecida comoautistaautistasperturbação do espectro do autismo

Um grupo de condições que afetam o desenvolvimento e que inclui o autismo e a síndrome de Asperger. Os sinais e sintomas incluem dificuldade de comunicação, dificuldade para interagir socialmente e comportamentos repetitivos.

Última verificação: Fonte: sem afirmação sobre o SUS a verificarEm construçãohistóricoSugerir correção
Mantido por Agente Raras·Colaborar como especialista →

Introdução

O que você precisa saber de cara

💬
EM LINGUAGEM SIMPLES

O autismo é uma condição do desenvolvimento que envolve dificuldades na comunicação, nos relacionamentos interpessoais e na flexibilidade de rotinas. A família costuma notar atraso no início da fala, contato visual limitado e movimentos repetitivos, podendo haver também convulsões associadas. No Brasil, o SUS dispensa a risperidona em comprimidos e solução oral segundo protocolo oficial para quadros com comportamento agressivo associado. Contudo, a condição não está incluída na lista de protocolos clínicos oficiais dedicados especificamente a doenças raras do Ministério da Saúde.

📋
Informacoes curadas por IA — podem conter imprecisoes

Um grupo de condições que afetam o desenvolvimento e que inclui o autismo e a síndrome de Asperger. Os sinais e sintomas incluem dificuldade de comunicação, dificuldade para interagir socialmente e comportamentos repetitivos.

Pesquisas ativas
256 ensaios
1012 total registrados no ClinicalTrials.gov
Publicações científicas
51 artigos
Último publicado: 2026 Apr 10
🏥
SUS: Sem cobertura SUSScore: 20%
CID-10: F84.0
Você se identifica com essa condição?
O Raras está aqui pra te apoiar — com ou sem diagnóstico

Encontrou um erro ou informação desatualizada? Sugira uma correção →

Entender a doença

Do básico ao detalhe, leia no seu ritmo

Preparando trilha educativa...

Sinais e sintomas

O que aparece no corpo e com que frequência cada sintoma acontece

Partes do corpo afetadas

🧠
Neurológico
5 sintomas
🦴
Ossos e articulações
1 sintomas

+ 6 sintomas em outras categorias

Características mais comuns

—
Atraso no desenvolvimento da fala e da linguagem
—
Capacidade prejudicada de formar relacionamentos com pares
—
Comportamento restritivo
—
Maneirismos repetitivos anormais
—
Uso prejudicado de comportamentos não verbais
—
Adesão inflexível a rotinas
12sintomas
Sem dados (12)

Os sintomas variam de pessoa para pessoa. Abaixo estão as 12 características clínicas mais associadas, ordenadas por frequência.

Atraso no desenvolvimento da fala e da linguagemDelayed speech and language development
Capacidade prejudicada de formar relacionamentos com paresImpaired ability to form peer relationships
Comportamento restritivoRestrictive behavior
Maneirismos repetitivos anormaisAbnormal repetitive mannerisms
Uso prejudicado de comportamentos não verbaisImpaired use of nonverbal behaviors

Linha do tempo da pesquisa

Publicações por ano — veja quando o interesse científico cresceu
Anos de pesquisa11
Total histórico51PubMed
Últimos 10 anos68publicações
Pico201810 papers
Linha do tempo
20202015Hoje · 2026🧪 1997Primeiro ensaio clínico📈 2018Ano de pico
Publicações por ano (últimos 10 anos)

Encontrou um erro ou informação desatualizada? Sugira uma correção →

Genética e causas

O que está alterado no DNA e como passa nas famílias

🧬

Nenhum gene associado encontrado

Os dados genéticos desta condição ainda estão sendo catalogados.

Diagnóstico

Os sinais que médicos procuram e os exames que confirmam

Carregando...

Tratamento e manejo

Remédios, cuidados de apoio e o que precisa acompanhar

Pipeline de tratamentos
Pipeline regulatório — de medicamentos já aprovados a drogas em pesquisa exploratória.
✓Aprovado2
3Fase 31
2Fase 26
1Fase 14
·Pré-clínico87
Medicamentos catalogadosEnsaios clínicos· 0 medicamentos · 100 ensaios
Carregando informações de tratamento...

Onde tratar no SUS

Hospitais de referência no Brasil e o protocolo oficial do SUS (PCDT)

🇧🇷 Atendimento SUS — Autismo

Centros de Referência SUS

13 centros habilitados pelo SUS para Autismo

Centros para Autismo

Detalhes dos centros

Hospital Infantil Albert Sabin

R. Tertuliano Sales, 544 - Vila União, Fortaleza - CE, 60410-794 · CNES 2407876

Serviço de Referência

Rota
Anomalias CongênitasDeficiência Intelectual

Hospital de Apoio de Brasília (HAB)

AENW 3 Lote A Setor Noroeste - Plano Piloto, Brasília - DF, 70684-831 · CNES 0010456

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital Estadual Infantil e Maternidade Alzir Bernardino Alves (HIABA)

Av. Min. Salgado Filho, 918 - Soteco, Vila Velha - ES, 29106-010 · CNES 6631207

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital das Clínicas da UFMG

Av. Prof. Alfredo Balena, 110 - Santa Efigênia, Belo Horizonte - MG, 30130-100 · CNES 2280167

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital Universitário João de Barros Barreto

R. dos Mundurucus, 4487 - Guamá, Belém - PA, 66073-000 · CNES 2337878

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Instituto de Medicina Integral Prof. Fernando Figueira (IMIP)

R. dos Coelhos, 300 - Boa Vista, Recife - PE, 50070-902 · CNES 0000647

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital Pequeno Príncipe

R. Des. Motta, 1070 - Água Verde, Curitiba - PR, 80250-060 · CNES 3143805

Serviço de Referência

Rota
Anomalias CongênitasDeficiência Intelectual

Hospital de Clínicas da UFPR

R. Gen. Carneiro, 181 - Alto da Glória, Curitiba - PR, 80060-900 · CNES 2364980

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Instituto Nacional de Saúde da Mulher, da Criança e do Adolescente Fernandes Figueira (IFF/Fiocruz)

Av. Rui Barbosa, 716 - Flamengo, Rio de Janeiro - RJ, 22250-020 · CNES 2269988

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital de Clínicas de Porto Alegre (HCPA)

Rua Ramiro Barcelos, 2350 Bloco A - Av. Protásio Alves, 211 - Bloco B e C - Santa Cecília, Porto Alegre - RS, 90035-903 · CNES 2237601

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital das Clínicas da FMUSP

R. Dr. Ovídio Pires de Campos, 225 - Cerqueira César, São Paulo - SP, 05403-010 · CNES 2077485

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital de Clínicas da UNICAMP

R. Vital Brasil, 251 - Cidade Universitária, Campinas - SP, 13083-888 · CNES 2748223

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital de Clínicas de Ribeirão Preto (HCRP-USP)

R. Ten. Catão Roxo, 3900 - Vila Monte Alegre, Ribeirão Preto - SP, 14015-010 · CNES 2082187

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual
Sobre os centros SUS: Estes centros são habilitados pelo Ministério da Saúde como Serviços de Referência em Doenças Raras ou Serviços de Atenção Especializada. O atendimento é pelo SUS, com encaminhamento da rede de atenção básica.

Dados de DATASUS/CNES, SBGM, ABNeuro e Ministério da Saúde. Sempre confirme a disponibilidade diretamente com o estabelecimento.

Pesquisa ativa

Ensaios clínicos abertos e novidades científicas recentes

Onde estão os ensaios

Com ensaio aberto em 37 países. O ponto verde marca onde há vaga agora.

🟢 Recrutando agora

100 pesquisas recrutando participantes. Converse com seu médico sobre a possibilidade de participar.

NCT07624448 · Regulating Together for Intellectual Disability and Autism: …Recrutando
NA🇺🇸 Estados Unidos
NCT07856927 · To Share or Not To Share: Navigating Disclosure and Stigma A…Recrutando
NA🇺🇸 Estados Unidos
NCT07630376 · Evaluating a Workbook to Promote Autistic WellbeingRecrutando
NA🇬🇧 Reino Unido
NCT07439042 · Buspirone for Anxiety in Autistic YouthRecrutando
PHASE4🇺🇸 Estados Unidos
NCT07812870 · Behavioral Activation for Treatment of Depression in Autisti…Recrutando
NA🇺🇸 Estados Unidos
NCT06934915 · Prednisone in Adults With an Immune-Mediated Subtype of Auti…Recrutando
EARLY_PHASE1🇺🇸 Estados Unidos
NCT07798297 · Transitional Intervention for Hyperacusis in AutismRecrutando
NA🇺🇸 Estados Unidos
NCT07476937 · Differences in Rest, Emotion, and Arousal Modulation in Yout…Recrutando
NA🇺🇸 Estados Unidos
NCT07427810 · Follow-up of Adolescents With Autism and Psychotic Symptoms …Recrutando
🇸🇪 Suécia
NCT07642661 · A Placebo-controlled Trial of Folinic Acid in Children With …Recrutando
PHASE2🇮🇱 Israel
NCT07435740 · Parent-Mediated Telehealth Intervention for Insomnia in Youn…Recrutando
NA🇺🇸 Estados Unidos
NCT07622316 · GAIP ASD Research StudyRecrutando
PHASE1🇺🇸 Estados Unidos
NCT07738003 · Perinatal Autism Genetics and Epigenetics StudyRecrutando
🇺🇸 Estados Unidos
NCT07572110 · Project IndependenceRecrutando
NA🇺🇸 Estados Unidos
NCT07420478 · TF-CBT for Autistic Youth Pilot Implementation - Open PilotRecrutando
NA🇺🇸 Estados Unidos
NCT07304440 · Adia Med of Winter Park LLC Autism Spectrum Disorder Researc…Recrutando
PHASE1🇺🇸 Estados Unidos
NCT07539519 · A Toolkit to Improve Mental Health Treatment for Autistic In…Recrutando
NA🇺🇸 Estados Unidos
NCT07042347 · Testing a Measurement Feedback App to Improve Data Quality, …Recrutando
NA🇺🇸 Estados Unidos
NCT07216196 · The Feasibility of a Remote Problem-Solving Intervention for…Recrutando
NA🇺🇸 Estados Unidos
NCT07424404 · A Study to Evaluate the Long-term Safety and Tolerability of…Recrutando
PHASE3🇦🇺 Austrália · 🇨🇦 Canadá · 🇫🇷 França +7
NCT07069413 · Sibwatch: Optimizing Intervention Options for Infants and To…Recrutando
NA🇺🇸 Estados Unidos
NCT07406100 · Piloting the Competence in Romance and Understanding Sexual …Recrutando
NA🇺🇸 Estados Unidos
NCT07500363 · Improving Caregiver Engagement in Early InterventionsRecrutando
NA🇺🇸 Estados Unidos
NCT07533331 · Testing Conversational Agents as a Digital CompanionRecrutando
NA🇺🇸 Estados Unidos
NCT07471594 · Family-Centered Implementation of Parent Training for Autist…Recrutando
NA🇺🇸 Estados Unidos
NCT07421830 · An Empowering Parent Training Intervention to Increase Physi…Recrutando
NA🇺🇸 Estados Unidos
NCT07367256 · Using Virtual Reality to Improve Emotion Understanding in Ch…Recrutando
NA🇮🇹 Itália
NCT07432776 · Effect of an 8-Week Pickleball Program for Adults With Autis…Recrutando
EARLY_PHASE1🇺🇸 Estados Unidos
NCT06853665 · The TEAM Study - Treatment Efficacy for Autism/Attention Usi…Recrutando
PHASE4🇺🇸 Estados Unidos
NCT07276750 · Coaching and Leadership in Autism Support SettingsRecrutando
NA🇺🇸 Estados Unidos
NCT06523387 · Online Pivotal Response Treatment Training in Autism Spectru…Recrutando
NA🇺🇸 Estados Unidos
NCT07091279 · Propranolol for Aggression, Self-Injury, and Severe Disrupti…Recrutando
PHASE2🇺🇸 Estados Unidos
NCT07531914 · Five Digits Test - Validation of a Neuropsychological Test o…Recrutando
🇸🇪 Suécia
NCT07222982 · Social Groups for Autistic Young Adults (SDARIYA)Recrutando
NA🇺🇸 Estados Unidos
NCT07403396 · Static Balance Assessment in Children With ASD Using VRRSRecrutando
🇮🇹 Itália
NCT07315867 · Better Social, Emotional Communication, Healthy Relationship…Recrutando
NA🇺🇸 Estados Unidos
NCT07329257 · Investigating Phenotypic, Epigenetic, and NeuroGenetic Trait…Recrutando
🇺🇸 Estados Unidos
NCT07238153 · Promoting Emotional and Autonomic Control Through Guided Bre…Recrutando
NA🇧🇪 Bélgica
NCT07248254 · Effects Of DPPT On Motor Skills And Sleep In Children With A…Recrutando
NAPakistan
NCT07302048 · Impact and Determinants of Success of a Mobile Multidiscipli…Recrutando
NA🇫🇷 França
NCT07262853 · Dual Executive Function Training PackageRecrutando
NAHong Kong
NCT07199218 · Placebo-Controlled Study of Terpenes-Enriched Cannabis Oil T…Recrutando
PHASE2🇮🇱 Israel
NCT05999240 · Pimavanserin for Rigid-compulsive Symptoms in Autism Spectru…Recrutando
PHASE2🇺🇸 Estados Unidos
NCT07054866 · Rural Autistic Individuals - Supporting ExpressionRecrutando
NA🇺🇸 Estados Unidos
NCT06733584 · Meeting the Needs of Young Hispanic Autistic ChildrenRecrutando
NA🇺🇸 Estados Unidos
NCT07148258 · Evaluating Georgia Part C Implementation OutcomesRecrutando
NA🇺🇸 Estados Unidos
NCT07203469 · Where Wild Things Grow: Nature- and Activity-based Group Int…Recrutando
NA🇳🇴 Noruega
NCT07081724 · "Opt-In" Early Intervention Program for Children Waiting to …Recrutando
NA🇺🇸 Estados Unidos
NCT07084324 · Spanish-language Executive Function Intervention for Childre…Recrutando
NA🇺🇸 Estados Unidos
NCT06386029 · The Power Down Pilot Study: A Novel Bedtime Manipulation Pro…Recrutando
NA🇺🇸 Estados Unidos
NCT07708246 · Parent-Mediated Social Cognition Intervention for Young Chil…Recrutando
NA🇨🇳 China
NCT06526208 · Investigating a Marijuana-based Compound as a Treatment for …Recrutando
PHASE2🇺🇸 Estados Unidos
NCT06909279 · Caregiver Training to Support Children With Social Communica…Recrutando
NA🇨🇦 Canadá
NCT06904508 · Brain Activity Changes After Cognitive Behavioral Therapy fo…Recrutando
NA🇺🇸 Estados Unidos
NCT07027319 · The Effect of Triple P Training on Children's Repetitive Beh…Recrutando
NATurkey (Türkiye)
NCT06920615 · Stereotypic Behaviors and Feeding Difficulties in Adults Wit…Recrutando
NA🇳🇴 Noruega
NCT06908174 · Differences in Prosocial Behaviors and Related Brain Network…Recrutando
🇨🇳 China
NCT06923553 · Implementation of Naturalistic Developmental Behavioral Inte…Recrutando
NA🇺🇸 Estados Unidos
NCT07136636 · Speech of Kids After Neonatal EncephalopathyRecrutando
Hungary
NCT06859918 · Randomized Clinical Trial of TUNE In 3.0: A Social/Emotional…Recrutando
NA🇺🇸 Estados Unidos
NCT06893718 · Treadmill Training With and Without Compression Stockings on…Recrutando
NAPakistan
NCT06872229 · The Impact of Sensory Integration on Attention in AutismRecrutando
🇮🇹 Itália
NCT06876857 · University of Central Florida CereBankRecrutando
🇺🇸 Estados Unidos
NCT06391684 · Flexibility and the Predictive Brain in Autistic Males and F…Recrutando
🇫🇷 França
NCT07590973 · Online Evaluation of the Diagnostic Accuracy of BlinkLab's D…Recrutando
🇺🇸 Estados Unidos
NCT06627205 · Sleep Restriction Therapy (SRT) for Sleep Problems in Childr…Recrutando
NA🇺🇸 Estados Unidos
NCT06703125 · The Alama Project: Autism Outcomes and Neurobehavioral Marke…Recrutando
NAKenya
NCT07061119 · Effect of Cawthorne Cooksey Exercises on Balance in Autistic…Recrutando
NAPakistan
NCT06471504 · Use of Eye Tracking to Aid in Autism Risk DetectionRecrutando
NA🇺🇸 Estados Unidos
NCT06472115 · Parent-Mediated Intervention Targeting Insistence on Samenes…Recrutando
NA🇺🇸 Estados Unidos
NCT06705907 · Improving Academic and Social Functioning in Middle-Schooler…Recrutando
NA🇺🇸 Estados Unidos
NCT05853861 · Promoting Early Intervention Timing and Attention to Languag…Recrutando
NA🇺🇸 Estados Unidos
NCT06732219 · A Single-Arm Pilot Trial for Mitigating Relapse of Severe Pr…Recrutando
NA🇺🇸 Estados Unidos
NCT06234501 · Testing the Efficacy of 100mg Vitamin-B6 Daily for Sensory R…Recrutando
NA🇬🇧 Reino Unido
NCT06930417 · Characterization and Natural History of Williams Syndrome an…Recrutando
🇺🇸 Estados Unidos
NCT07137273 · Optimizing Dimensions of ReinforcementRecrutando
NA🇺🇸 Estados Unidos
NCT06649916 · Word Learning From Parentese in Autistic ChildrenRecrutando
NA🇺🇸 Estados Unidos
NCT06668519 · Magnetoencephalography in ChildrenRecrutando
🇨🇳 China
NCT06081348 · Sertraline vs. Placebo in the Treatment of Anxiety in Childr…Recrutando
PHASE2🇨🇦 Canadá
NCT06127472 · Psychoeducation for Older Adults With AutismRecrutando
NA🇳🇱 Países Baixos
NCT06656585 · Exploring Virtual Reality As an Intervention for Food Select…Recrutando
NA🇮🇹 Itália
NCT06723522 · High Definition Transcranial Direct Current Stimulation of R…Recrutando
NA🇨🇳 China
NCT06362733 · Modified Pivotal Response Treatment for Insistence on Samene…Recrutando
NA🇺🇸 Estados Unidos
NCT06506097 · Family-school Partnership Intervention for Early Childhood E…Recrutando
NA🇺🇸 Estados Unidos
NCT07389720 · Characterization of (A)Typical Sensorimotor Pathways in Indi…Recrutando
NA🇮🇹 Itália
NCT07768332 · Assessing Outcomes of Three Different Museum-based Social Pr…Recrutando
NA🇹🇼 Taiwan
NCT05066178 · Speech Treatment for Minimally Verbal Children With ASD and …Recrutando
NA🇺🇸 Estados Unidos
NCT06399952 · Baker Gordon Syndrome Natural History StudyRecrutando
🇺🇸 Estados Unidos
NCT06497920 · rTMS to Improve Motor Function in AutismRecrutando
NA🇨🇦 Canadá
NCT06329245 · Development of Prosocial Behaviors and Related Brain Network…Recrutando
🇨🇳 China
NCT06495684 · Effects of Multiple-Session Transcranial Direct Current Stim…Recrutando
NA🇺🇸 Estados Unidos
NCT06726187 · DSM-5 Personality Disorders in Adults With AutismRecrutando
🇳🇱 Países Baixos
NCT06005285 · Examining the Effectiveness of the Early Start Denver Model …Recrutando
NA🇺🇸 Estados Unidos
NCT06208722 · Testing a Mobile App to Improve Toothbrushing Skills and Hab…Recrutando
NA🇺🇸 Estados Unidos
NCT07101523 · Using Technologies to Promote HEalthy Lifestyles in Adolesce…Recrutando
NA🇪🇸 Espanha
NCT07134569 · Motor Function Assessment and VR-based Motor Training in Adu…Recrutando
NA🇹🇼 Taiwan
NCT06443320 · Evaluation of the Videodrama Therapeutic Device for Children…Recrutando
NA🇫🇷 França
NCT06309160 · COMPASS Across Settings (CAST) for Improving Transition Outc…Recrutando
NA🇺🇸 Estados Unidos
NCT06016621 · Autism - Children's Improvisational Music Therapy EvaluationRecrutando
NA🇬🇧 Reino Unido
NCT05726708 · Impact of an E-Learning Coaching for Parents of Young Childr…Recrutando
NA🇨🇭 Suíça

Outros ensaios clínicos

🧪 Está conduzindo uma pesquisa?
Divulgue para pacientes e familiares que acompanham esta doença.
Divulgar pesquisa →

Publicações mais relevantes

Timeline de publicações
44 papers (10 anos)
#1

Global burden of lower respiratory infections and aetiologies, 1990-2023: a systematic analysis for the Global Burden of Disease Study 2023.

The Lancet. Infectious diseases2025 Dec 15

Lower respiratory infections (LRIs) remain the world's leading infectious cause of death. This analysis from the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2023 provides global, regional, and national estimates of LRI incidence, mortality, and disability-adjusted life-years (DALYs), with attribution to 26 pathogens, including 11 newly modelled pathogens, across 204 countries and territories from 1990 to 2023. With new data and revised modelling techniques, these estimates serve as an update and expansion to GBD 2021. Through these estimates, we also aimed to assess progress towards the 2025 Global Action Plan for the Prevention and Control of Pneumonia and Diarrhoea (GAPPD) target for pneumonia mortality in children younger than 5 years. Mortality from LRIs, defined as physician-diagnosed pneumonia or bronchiolitis, was estimated using the Cause of Death Ensemble model with data from vital registration, verbal autopsy, surveillance, and minimally invasive tissue sampling. The Bayesian meta-regression tool DisMod-MR 2.1 was used to model overall morbidity due to LRIs. DALYs were calculated as the sum of years of life lost (YLLs) and years lived with disability (YLDs) for all locations, years, age groups, and sexes. We modelled pathogen-specific case-fatality ratios (CFRs) for each age group and location using splined binomial regression to create internally consistent estimates of incidence and mortality proportions attributable to viral, fungal, parasitic, and bacterial pathogens. Progress was assessed towards the GAPPD target of less than three deaths from pneumonia per 1000 livebirths, which is roughly equivalent to a mortality rate of less than 60 deaths per 100 000 children younger than 5 years. In 2023, LRIs were responsible for 2·50 million (95% uncertainty interval [UI] 2·24-2·81) deaths and 98·7 million (87·7-112) DALYs, with children younger than 5 years and adults aged 70 years and older carrying the highest burden. LRI mortality in children younger than 5 years fell by 33·4% (10·4-47·4) since 2010, with a global mortality rate of 94·8 (75·6-116·4) per 100 000 person-years in 2023. Among adults aged 70 years and older, the burden remained substantial with only marginal declines since 2010. A mortality rate of less than 60 deaths per 100 000 for children younger than 5 years was met by 129 of the 204 modelled countries in 2023. At a super-regional level, sub-Saharan Africa had an aggregate mortality rate in children younger than 5 years (hereafter referred to as under-5 mortality rate) furthest from the GAPPD target. Streptococcus pneumoniae continued to account for the largest number of LRI deaths globally (634 000 [95% UI 565 000-721 000] deaths or 25·3% [24·5-26·1] of all LRI deaths), followed by Staphylococcus aureus (271 000 [243 000-298 000] deaths or 10·9% [10·3-11·3]), and Klebsiella pneumoniae (228 000 [204 000-261 000] deaths or 9·1% [8·8-9·5]). Among pathogens newly modelled in this study, non-tuberculous mycobacteria (responsible for 177 000 [95% UI 155 000-201 000] deaths) and Aspergillus spp (responsible for 67 800 [59 900-75 900] deaths) emerged as important contributors. Altogether, the 11 newly modelled pathogens accounted for approximately 22% of LRI deaths. This comprehensive analysis underscores both the gains achieved through vaccination and the challenges that remain in controlling the LRI burden globally. Furthermore, it demonstrates persistent disparities in disease burden, with the highest mortality rates concentrated in countries in sub-Saharan Africa. Globally, as well as in these high-burden locations, the under-5 LRI mortality rate remains well above the GAPPD target. Progress towards this target requires equitable access to vaccines and preventive therapies-including newer interventions such as respiratory syncytial virus monoclonal antibodies-and health systems capable of early diagnosis and treatment. Expanding surveillance of emerging pathogens, strengthening adult immunisation programmes, and combating vaccine hesitancy are also crucial. As the global population ages, the dual challenge of sustaining gains in child survival while addressing the rising vulnerability in older adults will shape future pneumonia control strategies. Gates Foundation.

#2

Global burden of 292 causes of death in 204 countries and territories and 660 subnational locations, 1990-2023: a systematic analysis for the Global Burden of Disease Study 2023.

Lancet (London, England)2025 Oct 18

Timely and comprehensive analyses of causes of death stratified by age, sex, and location are essential for shaping effective health policies aimed at reducing global mortality. The Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2023 provides cause-specific mortality estimates measured in counts, rates, and years of life lost (YLLs). GBD 2023 aimed to enhance our understanding of the relationship between age and cause of death by quantifying the probability of dying before age 70 years (70q0) and the mean age at death by cause and sex. This study enables comparisons of the impact of causes of death over time, offering a deeper understanding of how these causes affect global populations. GBD 2023 produced estimates for 292 causes of death disaggregated by age-sex-location-year in 204 countries and territories and 660 subnational locations for each year from 1990 until 2023. We used a modelling tool developed for GBD, the Cause of Death Ensemble model (CODEm), to estimate cause-specific death rates for most causes. We computed YLLs as the product of the number of deaths for each cause-age-sex-location-year and the standard life expectancy at each age. Probability of death was calculated as the chance of dying from a given cause in a specific age period, for a specific population. Mean age at death was calculated by first assigning the midpoint age of each age group for every death, followed by computing the mean of all midpoint ages across all deaths attributed to a given cause. We used GBD death estimates to calculate the observed mean age at death and to model the expected mean age across causes, sexes, years, and locations. The expected mean age reflects the expected mean age at death for individuals within a population, based on global mortality rates and the population's age structure. Comparatively, the observed mean age represents the actual mean age at death, influenced by all factors unique to a location-specific population, including its age structure. As part of the modelling process, uncertainty intervals (UIs) were generated using the 2·5th and 97·5th percentiles from a 250-draw distribution for each metric. Findings are reported as counts and age-standardised rates. Methodological improvements for cause-of-death estimates in GBD 2023 include a correction for the misclassification of deaths due to COVID-19, updates to the method used to estimate COVID-19, and updates to the CODEm modelling framework. This analysis used 55 761 data sources, including vital registration and verbal autopsy data as well as data from surveys, censuses, surveillance systems, and cancer registries, among others. For GBD 2023, there were 312 new country-years of vital registration cause-of-death data, 3 country-years of surveillance data, 51 country-years of verbal autopsy data, and 144 country-years of other data types that were added to those used in previous GBD rounds. The initial years of the COVID-19 pandemic caused shifts in long-standing rankings of the leading causes of global deaths: it ranked as the number one age-standardised cause of death at Level 3 of the GBD cause classification hierarchy in 2021. By 2023, COVID-19 dropped to the 20th place among the leading global causes, returning the rankings of the leading two causes to those typical across the time series (ie, ischaemic heart disease and stroke). While ischaemic heart disease and stroke persist as leading causes of death, there has been progress in reducing their age-standardised mortality rates globally. Four other leading causes have also shown large declines in global age-standardised mortality rates across the study period: diarrhoeal diseases, tuberculosis, stomach cancer, and measles. Other causes of death showed disparate patterns between sexes, notably for deaths from conflict and terrorism in some locations. A large reduction in age-standardised rates of YLLs occurred for neonatal disorders. Despite this, neonatal disorders remained the leading cause of global YLLs over the period studied, except in 2021, when COVID-19 was temporarily the leading cause. Compared to 1990, there has been a considerable reduction in total YLLs in many vaccine-preventable diseases, most notably diphtheria, pertussis, tetanus, and measles. In addition, this study quantified the mean age at death for all-cause mortality and cause-specific mortality and found noticeable variation by sex and location. The global all-cause mean age at death increased from 46·8 years (95% UI 46·6-47·0) in 1990 to 63·4 years (63·1-63·7) in 2023. For males, mean age increased from 45·4 years (45·1-45·7) to 61·2 years (60·7-61·6), and for females it increased from 48·5 years (48·1-48·8) to 65·9 years (65·5-66·3), from 1990 to 2023. The highest all-cause mean age at death in 2023 was found in the high-income super-region, where the mean age for females reached 80·9 years (80·9-81·0) and for males 74·8 years (74·8-74·9). By comparison, the lowest all-cause mean age at death occurred in sub-Saharan Africa, where it was 38·0 years (37·5-38·4) for females and 35·6 years (35·2-35·9) for males in 2023. Lastly, our study found that all-cause 70q0 decreased across each GBD super-region and region from 2000 to 2023, although with large variability between them. For females, we found that 70q0 notably increased from drug use disorders and conflict and terrorism. Leading causes that increased 70q0 for males also included drug use disorders, as well as diabetes. In sub-Saharan Africa, there was an increase in 70q0 for many non-communicable diseases (NCDs). Additionally, the mean age at death from NCDs was lower than the expected mean age at death for this super-region. By comparison, there was an increase in 70q0 for drug use disorders in the high-income super-region, which also had an observed mean age at death lower than the expected value. We examined global mortality patterns over the past three decades, highlighting-with enhanced estimation methods-the impacts of major events such as the COVID-19 pandemic, in addition to broader trends such as increasing NCDs in low-income regions that reflect ongoing shifts in the global epidemiological transition. This study also delves into premature mortality patterns, exploring the interplay between age and causes of death and deepening our understanding of where targeted resources could be applied to further reduce preventable sources of mortality. We provide essential insights into global and regional health disparities, identifying locations in need of targeted interventions to address both communicable and non-communicable diseases. There is an ever-present need for strengthened health-care systems that are resilient to future pandemics and the shifting burden of disease, particularly among ageing populations in regions with high mortality rates. Robust estimates of causes of death are increasingly essential to inform health priorities and guide efforts toward achieving global health equity. The need for global collaboration to reduce preventable mortality is more important than ever, as shifting burdens of disease are affecting all nations, albeit at different paces and scales. Gates Foundation.

#3

Burden of 375 diseases and injuries, risk-attributable burden of 88 risk factors, and healthy life expectancy in 204 countries and territories, including 660 subnational locations, 1990-2023: a systematic analysis for the Global Burden of Disease Study 2023.

Lancet (London, England)2025 Oct 18

For more than three decades, the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) has provided a framework to quantify health loss due to diseases, injuries, and associated risk factors. This paper presents GBD 2023 findings on disease and injury burden and risk-attributable health loss, offering a global audit of the state of world health to inform public health priorities. This work captures the evolving landscape of health metrics across age groups, sexes, and locations, while reflecting on the remaining post-COVID-19 challenges to achieving our collective global health ambitions. The GBD 2023 combined analysis estimated years lived with disability (YLDs), years of life lost (YLLs), and disability-adjusted life-years (DALYs) for 375 diseases and injuries, and risk-attributable burden associated with 88 modifiable risk factors. Of the more than 310 000 total data sources used for all GBD 2023 (about 30% of which were new to this estimation round), more than 120 000 sources were used for estimation of disease and injury burden and 59 000 for risk factor estimation, and included vital registration systems, surveys, disease registries, and published scientific literature. Data were analysed using previously established modelling approaches, such as disease modelling meta-regression version 2.1 (DisMod-MR 2.1) and comparative risk assessment methods. Diseases and injuries were categorised into four levels on the basis of the established GBD cause hierarchy, as were risk factors using the GBD risk hierarchy. Estimates stratified by age, sex, location, and year from 1990 to 2023 were focused on disease-specific time trends over the 2010-23 period and presented as counts (to three significant figures) and age-standardised rates per 100 000 person-years (to one decimal place). For each measure, 95% uncertainty intervals [UIs] were calculated with the 2·5th and 97·5th percentile ordered values from a 250-draw distribution. Total numbers of global DALYs grew 6·1% (95% UI 4·0-8·1), from 2·64 billion (2·46-2·86) in 2010 to 2·80 billion (2·57-3·08) in 2023, but age-standardised DALY rates, which account for population growth and ageing, decreased by 12·6% (11·0-14·1), revealing large long-term health improvements. Non-communicable diseases (NCDs) contributed 1·45 billion (1·31-1·61) global DALYs in 2010, increasing to 1·80 billion (1·63-2·03) in 2023, alongside a concurrent 4·1% (1·9-6·3) reduction in age-standardised rates. Based on DALY counts, the leading level 3 NCDs in 2023 were ischaemic heart disease (193 million [176-209] DALYs), stroke (157 million [141-172]), and diabetes (90·2 million [75·2-107]), with the largest increases in age-standardised rates since 2010 occurring for anxiety disorders (62·8% [34·0-107·5]), depressive disorders (26·3% [11·6-42·9]), and diabetes (14·9% [7·5-25·6]). Remarkable health gains were made for communicable, maternal, neonatal, and nutritional (CMNN) diseases, with DALYs falling from 874 million (837-917) in 2010 to 681 million (642-736) in 2023, and a 25·8% (22·6-28·7) reduction in age-standardised DALY rates. During the COVID-19 pandemic, DALYs due to CMNN diseases rose but returned to pre-pandemic levels by 2023. From 2010 to 2023, decreases in age-standardised rates for CMNN diseases were led by rate decreases of 49·1% (32·7-61·0) for diarrhoeal diseases, 42·9% (38·0-48·0) for HIV/AIDS, and 42·2% (23·6-56·6) for tuberculosis. Neonatal disorders and lower respiratory infections remained the leading level 3 CMNN causes globally in 2023, although both showed notable rate decreases from 2010, declining by 16·5% (10·6-22·0) and 24·8% (7·4-36·7), respectively. Injury-related age-standardised DALY rates decreased by 15·6% (10·7-19·8) over the same period. Differences in burden due to NCDs, CMNN diseases, and injuries persisted across age, sex, time, and location. Based on our risk analysis, nearly 50% (1·27 billion [1·18-1·38]) of the roughly 2·80 billion total global DALYs in 2023 were attributable to the 88 risk factors analysed in GBD. Globally, the five level 3 risk factors contributing the highest proportion of risk-attributable DALYs were high systolic blood pressure (SBP), particulate matter pollution, high fasting plasma glucose (FPG), smoking, and low birthweight and short gestation-with high SBP accounting for 8·4% (6·9-10·0) of total DALYs. Of the three overarching level 1 GBD risk factor categories-behavioural, metabolic, and environmental and occupational-risk-attributable DALYs rose between 2010 and 2023 only for metabolic risks, increasing by 30·7% (24·8-37·3); however, age-standardised DALY rates attributable to metabolic risks decreased by 6·7% (2·0-11·0) over the same period. For all but three of the 25 leading level 3 risk factors, age-standardised rates dropped between 2010 and 2023-eg, declining by 54·4% (38·7-65·3) for unsafe sanitation, 50·5% (33·3-63·1) for unsafe water source, and 45·2% (25·6-72·0) for no access to handwashing facility, and by 44·9% (37·3-53·5) for child growth failure. The three leading level 3 risk factors for which age-standardised attributable DALY rates rose were high BMI (10·5% [0·1 to 20·9]), drug use (8·4% [2·6 to 15·3]), and high FPG (6·2% [-2·7 to 15·6]; non-significant). Our findings underscore the complex and dynamic nature of global health challenges. Since 2010, there have been large decreases in burden due to CMNN diseases and many environmental and behavioural risk factors, juxtaposed with sizeable increases in DALYs attributable to metabolic risk factors and NCDs in growing and ageing populations. This long-observed consequence of the global epidemiological transition was only temporarily interrupted by the COVID-19 pandemic. The substantially decreasing CMNN disease burden, despite the 2008 global financial crisis and pandemic-related disruptions, is one of the greatest collective public health successes known. However, these achievements are at risk of being reversed due to major cuts to development assistance for health globally, the effects of which will hit low-income countries with high burden the hardest. Without sustained investment in evidence-based interventions and policies, progress could stall or reverse, leading to widespread human costs and geopolitical instability. Moreover, the rising NCD burden necessitates intensified efforts to mitigate exposure to leading risk factors-eg, air pollution, smoking, and metabolic risks, such as high SBP, BMI, and FPG-including policies that promote food security, healthier diets, physical activity, and equitable and expanded access to potential treatments, such as GLP-1 receptor agonists. Decisive, coordinated action is needed to address long-standing yet growing health challenges, including depressive and anxiety disorders. Yet this can be only part of the solution. Our response to the NCD syndemic-the complex interaction of multiple health risks, social determinants, and systemic challenges-will define the future landscape of global health. To ensure human wellbeing, economic stability, and social equity, global action to sustain and advance health gains must prioritise reducing disparities by addressing socioeconomic and demographic determinants, ensuring equitable health-care access, tackling malnutrition, strengthening health systems, and improving vaccination coverage. We live in times of great opportunity. Gates Foundation and Bloomberg Philanthropies.

#4

Characterising acute and chronic care needs: insights from the Global Burden of Disease Study 2019.

Nature communications2025 May 07

Chronic care manages long-term, progressive conditions, while acute care addresses short-term conditions. Chronic conditions increasingly strain health systems, which are often unprepared for these demands. This study examines the burden of conditions requiring acute versus chronic care, including sequelae. Conditions and sequelae from the Global Burden of Diseases Study 2019 were classified into acute or chronic care categories. Data were analysed by age, sex, and socio-demographic index, presenting total numbers and contributions to burden metrics such as Disability-Adjusted Life Years (DALYs), Years Lived with Disability (YLD), and Years of Life Lost (YLL). Approximately 68% of DALYs were attributed to chronic care, while 27% were due to acute care. Chronic care needs increased with age, representing 86% of YLDs and 71% of YLLs, and accounting for 93% of YLDs from sequelae. These findings highlight that chronic care needs far exceed acute care needs globally, necessitating health systems to adapt accordingly.

#5

Paternal valproate use and impact of shared genetic susceptibility on child neurodevelopment.

Scientific reports2025 Nov 07

Paternal use of valproate during spermatogenesis has been associated with increased risk of neurodevelopmental disorders (NDDs) in offspring, yet the role of genetic confounding is unclear. Using data from the Norwegian Mother, Father, and Child Cohort Study (MoBa), we assessed genetic susceptibility to epilepsy, ADHD and autism spectrum disorders (ASD) in fathers with epilepsy treated with valproate (n = 41), lamotrigine or levetiracetam (n = 37), other anti-seizure medications (ASMs; n = 80), and healthy controls (n = 54,752). Fathers using valproate had significantly higher polygenic risk scores (PRSs) for epilepsy compared to those using lamotrigine or levetiracetam (mean difference: 0.66, 95% CI: 0.21-1.11, p ≈ 0.005), other ASMs (0.41, 95% CI: 0.02-0.81, p ≈ 0.04) and controls (0.85, 95% CI: 0.54-1.15, p = 5.8 × 10⁻⁸). No robust associations were found between paternal ASM use or epilepsy PRS and child neurodevelopmental outcomes. Significant genetic overlap was found among the top 1% of weighted SNPs in the PRSs for epilepsy, ADHD and ASD (428 genes, p ≈ 0.0001), enriched for neurodevelopmental pathways. These results emphasize the importance of considering shared genetic susceptibility when assessing risks of paternal valproate exposure.

Publicações recentes

Ver todas no PubMed

📚 EuropePMCmostrando 68

2025

Global burden of lower respiratory infections and aetiologies, 1990-2023: a systematic analysis for the Global Burden of Disease Study 2023.

The Lancet. Infectious diseases
2025

Paternal valproate use and impact of shared genetic susceptibility on child neurodevelopment.

Scientific reports
2025

Global burden of 292 causes of death in 204 countries and territories and 660 subnational locations, 1990-2023: a systematic analysis for the Global Burden of Disease Study 2023.

Lancet (London, England)
2025

Burden of 375 diseases and injuries, risk-attributable burden of 88 risk factors, and healthy life expectancy in 204 countries and territories, including 660 subnational locations, 1990-2023: a systematic analysis for the Global Burden of Disease Study 2023.

Lancet (London, England)
2025

Autism spectrum disorder in adulthood: Diagnostic and training challenges in Greece.

Psychiatrike = Psychiatriki
2025

Characterising acute and chronic care needs: insights from the Global Burden of Disease Study 2019.

Nature communications
2025

Atypical Resting-State EEG Graph Metrics of Network Efficiency Across Development in Autism and Their Association with Social Cognition: Results from the LEAP Study.

Journal of autism and developmental disorders
2024

Investigating social orienting in children with Phelan-McDermid syndrome and 'idiopathic' autism.

Journal of neurodevelopmental disorders
2025

A burden of rare copy number variants in obsessive-compulsive disorder.

Molecular psychiatry
2024

Enhanced motor noise in an autism subtype with poor motor skills.

Molecular autism
2024

Mid-childhood autism sibling recurrence in infants with a family history of autism.

Autism research : official journal of the International Society for Autism Research
2025

Evaluation of a medically coordinated care program in the management of autism.

L'Encephale
2024

Proposal for standardized prenatal assessment of fetal open dysraphisms by the European reference network for Intellectual disability, TeleHealth, Autism and Congenital Anomalies (ITHACA) and eUROGEN.

Prenatal diagnosis
2024

Pathways to epilepsy surgery in children with tuberous sclerosis complex-associated epilepsy.

Revue neurologique
2024

European Autism GEnomics Registry (EAGER): protocol for a multicentre cohort study and registry.

BMJ open
2024

Seizure freedom but not epilepsy surgery is associated with fewer neuropsychiatric difficulties in patients with tuberous sclerosis.

Epilepsy & behavior : E&B
2022

Description of the First Registered Case of Lopes-Maciel-Rodan Syndrome in Russia.

International journal of molecular sciences
2022

Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank.

Nature genetics
2022

SYNGAP1-related developmental and epileptic encephalopathy: The impact on daily life.

Epilepsy & behavior : E&B
2021

Dietary Patterns, Eating Behavior, and Nutrient Intakes of Spanish Preschool Children with Autism Spectrum Disorders.

Nutrients
2021

Today Is My Day: Analysis of the Awareness Campaigns' Impact on Functional Diversity in the Press, on Google, and on Twitter.

International journal of environmental research and public health
2021

Scurvy as an Alarm Bell of Autistic Spectrum Disorder in the First World: A Case Report of a 3-Year-Old Girl.

The American journal of case reports
2021

Psychiatric disorders in individuals with neurofibromatosis 1 in Denmark: A nationwide register-based cohort study.

American journal of medical genetics. Part A
2021

Genetic architecture of type 1 diabetes with low genetic risk score informed by 41 unreported loci.

Communications biology
2022

Childhood Disintegrative Disorder (CDD): Symptomatology of the Norwegian Patient Population and Parents' Experiences of Patient Regression.

Journal of autism and developmental disorders
2021

Neuropsychological study in 19 French patients with White-Sutton syndrome and POGZ mutations.

Clinical genetics
2020

Intrinsic excitation-inhibition imbalance affects medial prefrontal cortex differently in autistic men versus women.

eLife
2020

Explaining Age at Autism Spectrum Diagnosis in Children with Migrant and Non-Migrant Background in Austria.

Brain sciences
2020

Unemployment Trajectories and the Early Risk of Disability Pension among Young People with and without Autism Spectrum Disorder: A Nationwide Study in Sweden.

International journal of environmental research and public health
2020

An integrated analysis of rare CNV and exome variation in Autism Spectrum Disorder using the Infinium PsychArray.

Scientific reports
2020

Whole-exome sequencing of 81 individuals from 27 multiply affected bipolar disorder families.

Translational psychiatry
2020

Neurotoxicity by mercury is not associated with autism spectrum disorders in Spanish children.

Italian journal of pediatrics
2019

PAICS deficiency, a new defect of de novo purine synthesis resulting in multiple congenital anomalies and fatal outcome.

Human molecular genetics
2019

Maternal immigrant status and signs of neurodevelopmental problems in early childhood: The French representative ELFE birth cohort.

Autism research : official journal of the International Society for Autism Research
2019

Phenome-wide Burden of Copy-Number Variation in the UK Biobank.

American journal of human genetics
2019

The clinical benefit of array-based comparative genomic hybridization for detection of copy number variants in Czech children with intellectual disability and developmental delay.

BMC medical genomics
2020

Age of First Walking and Associations with Symptom Severity in Children with Suspected or Diagnosed Autism Spectrum Disorder.

Journal of autism and developmental disorders
2019

Eurosibs: Towards robust measurement of infant neurocognitive predictors of autism across Europe.

Infant behavior & development
2019

Truncating variant burden in high-functioning autism and pleiotropic effects of LRP1 across psychiatric phenotypes.

Journal of psychiatry & neuroscience : JPN
2019

Intracellular Aluminium in Inflammatory and Glial Cells in Cerebral Amyloid Angiopathy: A Case Report.

International journal of environmental research and public health
2019

Association of Rare Copy Number Variants With Risk of Depression.

JAMA psychiatry
2019

Identification of common genetic risk variants for autism spectrum disorder.

Nature genetics
2019

Cognitive performance and functional outcomes of carriers of pathogenic copy number variants: analysis of the UK Biobank.

The British journal of psychiatry : the journal of mental science
2018

Rare Copy Number Variations in a Chinese Cohort of Autism Spectrum Disorder.

Frontiers in genetics
2018

The Italian autism network (ITAN): a resource for molecular genetics and biomarker investigations.

BMC psychiatry
2020

Spanish Cultural Validation of the Modified Checklist for Autism in Toddlers, Revised.

Journal of autism and developmental disorders
2018

Exploration and characterisation of the phenotypic and genetic profiles of patients with early onset schizophrenia associated with autism spectrum disorder and their first-degree relatives: a French multicentre case series study protocol (GenAuDiss).

BMJ open
2018

Association of Autistic Traits With Depression From Childhood to Age 18 Years.

JAMA psychiatry
2018

Genome wide analysis of rare copy number variations in alcohol abuse or dependence.

Journal of psychiatric research
2018

De novo mutations in MED13, a component of the Mediator complex, are associated with a novel neurodevelopmental disorder.

Human genetics
2018

EU-AIMS Longitudinal European Autism Project (LEAP): the autism twin cohort.

Molecular autism
2018

Delineating the psychiatric and behavioral phenotype of recurrent 2q13 deletions and duplications.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics
2018

Screening for TSC1 and TSC2 mutations using NGS in Greek children with tuberous sclerosis syndrome.

European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
2018

Copy Number Variation Analysis of 100 Twin Pairs Enriched for Neurodevelopmental Disorders.

Twin research and human genetics : the official journal of the International Society for Twin Studies
2017

Reproductive fitness and genetic risk of psychiatric disorders in the general population.

Nature communications
2017

Medical history of discordant twins and environmental etiologies of autism.

Translational psychiatry
2017

Age and gender-related differences in emotional and behavioural problems and autistic features in children and adolescents with Down syndrome: a survey-based study of 674 individuals.

Journal of intellectual disability research : JIDR
2017

Increased Risk for Substance Use-Related Problems in Autism Spectrum Disorders: A Population-Based Cohort Study.

Journal of autism and developmental disorders
2016

Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsy.

BMC medical genetics
2016

Protocol for the development and validation of a questionnaire to assess concerning behaviours and mental health in individuals with autism spectrum disorders: the Assessment of Concerning Behaviour (ACB) scale.

BMJ open
2016

Parents' attitudes toward genetic research in autism spectrum disorder.

Psychiatric genetics
2015

Autism spectrum disorder in tuberous sclerosis complex: searching for risk markers.

Orphanet journal of rare diseases
2016

Psychiatric gene discoveries shape evidence on ADHD's biology.

Molecular psychiatry
2016

Mutation screening of SCN2A in schizophrenia and identification of a novel loss-of-function mutation.

Psychiatric genetics
2015

Mutation screening of the ubiquitin ligase gene RNF135 in French patients with autism.

Psychiatric genetics
2016

The landscape of copy number variations in Finnish families with autism spectrum disorders.

Autism research : official journal of the International Society for Autism Research
2016

Use of early intervention for young children with autism spectrum disorder across Europe.

Autism : the international journal of research and practice
2015

Acute behavioral crises in psychiatric inpatients with autism spectrum disorder (ASD): recognition of concomitant medical or non-ASD psychiatric conditions predicts enhanced improvement.

Research in developmental disabilities

Associações

Organizações que acompanham esta doença — pra ter apoio e orientação

Ainda não temos associações cadastradas para Autismo.

É de uma associação que acompanha esta doença? Fale com a gente →

Vai consultar um especialista? Confirme o registro dele no conselho.
Conselhos e sociedades

Doenças relacionadas

Doenças com sintomas parecidos — ajudam quem ainda está buscando diagnóstico

Perguntas frequentes

O que as famílias mais perguntam sobre esta doença — cada resposta com a fonte de onde saiu

Respostas geradas por IA a partir das fontes citadas

O autismo é classificado como uma condição duradoura do desenvolvimento neurobiológico. O manejo concentra-se na promoção do desenvolvimento comunicativo e no acompanhamento comportamental dos indivíduos.

Referências

Fontes citadas no texto, publicações do grafo e bases de dados usadas neste verbete

10 publicações do grafo RarasNet (PubMed) · 5 bases de dados. Títulos, periódicos e PMIDs vêm direto da fonte, sem intermediação de IA.

  1. ORPHA:106
    Orphanet
  2. Q38404
    Wikidata

Dados compilados pelo RarasNet a partir de fontes abertas (Orphanet, OMIM, MONDO, PubMed/EuropePMC, ClinicalTrials.gov, DATASUS, PCDT/MS). Este conteúdo é informativo e não substitui avaliação médica.

Citar este verbete

Raras. (s.d.). Autismo. Em Raras — Enciclopédia de Doenças Raras do Brasil. https://raras.org/doenca/autismo

Formato APA. Conteúdo sob CC BY 4.0 — reuso livre com atribuição.

Conteúdo mantido por Agente Raras · Médicos e pesquisadores podem colaborar

Autismo
Compêndio · Raras BR

Autismo

ORPHA:106 · MONDO:0005258
CID-10
F84.0 · Autismo infantil
Ensaios
256 ativos
MedGen
UMLS
C0004352
Wikidata
Wikipedia
Papers 10a

📋 Origem dos dados

Esta página agrega dados de fontes públicas e oficiais. Dados sobre cobertura no SUS (PCDT, CEAF) são verificados ativamente por agente proativo (ver badge no infobox). Demais dados têm atribuição de fonte + data da última sincronização — clique para abrir o original.

Doença rara (ontologia)
fonte: Orphanet
Identificador unificado
fonte: MONDO
Indexação biomédica
fonte: MeSH (NLM)
Dado público estruturado
fonte: Wikidata
Rara