questionsmedicales.fr
Virus
Virus à ADN
Adenoviridae
Mastadenovirus
Mastadenovirus : Questions médicales fréquentes
Termes MeSH sélectionnés :
Diagnostic
5
Infections virales
Adenovirus
Diagnostic médical
Tests de laboratoire
Adenovirus
Culture virale
Anticorps
Adenovirus
Sérologie
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Sensibilité
Symptômes
5
Symptômes
Infections virales
Adenovirus
Diarrhée
Adenovirus
Symptômes gastro-intestinaux
Contagiosité
Transmission
Adenovirus
Gravité
Infections virales
Adenovirus
Symptômes persistants
Fatigue
Adenovirus
Prévention
5
Prévention
Hygiène
Adenovirus
Vaccins
Adenovirus
Prévention
Transmission
Prévention
Adenovirus
Masques
Prévention
Adenovirus
Désinfection
Prévention
Adenovirus
Traitements
5
Traitement
Infections virales
Adenovirus
Antiviraux
Adenovirus
Traitement
Symptômes
Analgésiques
Adenovirus
Antibiotiques
Infections virales
Adenovirus
Consultation médicale
Complications
Adenovirus
Complications
5
Complications
Pneumonie
Adenovirus
Conjonctivite
Complications
Adenovirus
Immunodépression
Complications
Adenovirus
Mortalité
Complications
Adenovirus
Surveillance
Complications
Adenovirus
Facteurs de risque
5
Facteurs de risque
Immunodépression
Adenovirus
Saisonnalité
Infections virales
Adenovirus
Conditions de vie
Transmission
Adenovirus
Antécédents médicaux
Infections respiratoires
Adenovirus
Stress
Immunité
Adenovirus
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"@type": "Question",
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"name": "Faut-il éviter les lieux bondés pour prévenir l'infection ?",
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"@type": "Question",
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"@type": "Question",
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"@type": "Question",
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"@type": "Question",
"name": "Le Mastadenovirus peut-il causer des infections oculaires ?",
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"@type": "Question",
"name": "Les personnes immunodéprimées risquent-elles plus de complications ?",
"position": 23,
"acceptedAnswer": {
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"@type": "Question",
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"position": 24,
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}
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{
"@type": "Question",
"name": "Comment surveiller les complications d'une infection par Mastadenovirus ?",
"position": 25,
"acceptedAnswer": {
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}
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{
"@type": "Question",
"name": "Quels sont les facteurs de risque d'infection par Mastadenovirus ?",
"position": 26,
"acceptedAnswer": {
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"text": "Les jeunes enfants, les personnes âgées et les immunodéprimés sont à risque élevé."
}
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{
"@type": "Question",
"name": "La saison influence-t-elle les infections par Mastadenovirus ?",
"position": 27,
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}
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"@type": "Question",
"name": "Les conditions de vie surpeuplées augmentent-elles le risque ?",
"position": 28,
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"name": "Les antécédents d'infections respiratoires augmentent-ils le risque ?",
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"name": "Le stress peut-il affecter le risque d'infection par Mastadenovirus ?",
"position": 30,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, le stress peut affaiblir le système immunitaire et augmenter le risque."
}
}
]
}
]
}
Expert en Médecine, Optimisation des Parcours de Soins et Révision Médicale
Validation scientifique effectuée le 02/03/2025
Contenu vérifié selon les dernières recommandations médicales
6 publications dans cette catégorie
Affiliations :
Laboratório de Microbiologia Molecular, Universidade Feevale, ERS 239 no. 2755, Novo Hamburgo, RS, 93352-000, Brazil.
5 publications dans cette catégorie
Affiliations :
Laboratório de Microbiologia Molecular, Universidade Feevale, ERS 239 no. 2755, Novo Hamburgo, RS, 93352-000, Brazil.
Publications dans "Mastadenovirus" :
4 publications dans cette catégorie
Affiliations :
Laboratório de Microbiologia Molecular, Universidade Feevale, ERS 239 no. 2755, Novo Hamburgo, RS, 93352-000, Brazil.
Publications dans "Mastadenovirus" :
3 publications dans cette catégorie
Affiliations :
Laboratório de Microbiologia Molecular, Universidade Feevale, ERS 239 no. 2755, Novo Hamburgo, RS, 93352-000, Brazil. 0178103@feevale.br.
Publications dans "Mastadenovirus" :
3 publications dans cette catégorie
Affiliations :
Universidade Feevale, Instituto de Ciências da Saúde, Laboratório de Microbiologia Molecular, Novo Hamburgo, Rio Grande do Sul, Brazil.
Publications dans "Mastadenovirus" :
2 publications dans cette catégorie
Affiliations :
WHO WPRO Regional Reference Measles/Rubella Laboratory and NHC Key Laboratory of Medical Virology and Viral Diseases, National Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention, 155 Changbai Road, Changping District, Beijing, 102206, People's Republic of China.
Publications dans "Mastadenovirus" :
2 publications dans cette catégorie
Affiliations :
WHO WPRO Regional Reference Measles/Rubella Laboratory and NHC Key Laboratory of Medical Virology and Viral Diseases, National Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention, 155 Changbai Road, Changping District, Beijing, 102206, People's Republic of China.
Publications dans "Mastadenovirus" :
2 publications dans cette catégorie
Publications dans "Mastadenovirus" :
2 publications dans cette catégorie
Affiliations :
WHO WPRO Regional Reference Measles/Rubella Laboratory and NHC Key Laboratory of Medical Virology and Viral Diseases, National Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention, 155 Changbai Road, Changping District, Beijing, 102206, People's Republic of China. wenbo_xu1@aliyun.com.
Publications dans "Mastadenovirus" :
2 publications dans cette catégorie
Affiliations :
Laboratory of Comparative and Environmental Virology, Oswaldo Cruz Institute, FIOCRUZ, Rio de Janeiro, Brazil. lorena.macena@aluno.fiocruz.br.
Publications dans "Mastadenovirus" :
2 publications dans cette catégorie
Affiliations :
Laboratory of Comparative and Environmental Virology, Oswaldo Cruz Institute, FIOCRUZ, Rio de Janeiro, Brazil.
Publications dans "Mastadenovirus" :
2 publications dans cette catégorie
Affiliations :
Laboratory of Comparative and Environmental Virology, Oswaldo Cruz Institute, FIOCRUZ, Rio de Janeiro, Brazil.
Publications dans "Mastadenovirus" :
2 publications dans cette catégorie
Affiliations :
Laboratory of Comparative and Environmental Virology, Oswaldo Cruz Institute, FIOCRUZ, Rio de Janeiro, Brazil.
Publications dans "Mastadenovirus" :
2 publications dans cette catégorie
Affiliations :
Laboratory of Comparative and Environmental Virology, Oswaldo Cruz Institute, FIOCRUZ, Rio de Janeiro, Brazil.
Publications dans "Mastadenovirus" :
2 publications dans cette catégorie
Affiliations :
Laboratório Central da Secretaria de Saúde do Estado do Rio Grande do Sul, LACEN/SES-RS, Av. Ipiranga, 5400, Porto Alegre, RS, 90610-000, Brazil.
Publications dans "Mastadenovirus" :
2 publications dans cette catégorie
Affiliations :
Laboratório Central da Secretaria de Saúde do Estado do Rio Grande do Sul, LACEN/SES-RS, Av. Ipiranga, 5400, Porto Alegre, RS, 90610-000, Brazil.
Publications dans "Mastadenovirus" :
2 publications dans cette catégorie
Affiliations :
Laboratório Central da Secretaria de Saúde do Estado do Rio Grande do Sul, LACEN/SES-RS, Av. Ipiranga, 5400, Porto Alegre, RS, 90610-000, Brazil.
Publications dans "Mastadenovirus" :
2 publications dans cette catégorie
Affiliations :
Centro Estadual de Vigilância em Saúde da Secretaria de Saúde do Estado do Rio Grande do Sul-CEVS/SES-RS, Av. Ipiranga, 5400, Porto Alegre, RS, 90610-000, Brazil.
Publications dans "Mastadenovirus" :
2 publications dans cette catégorie
Affiliations :
Universidade Feevale, Instituto de Ciências da Saúde, Laboratório de Microbiologia Molecular, Novo Hamburgo, Rio Grande do Sul, Brazil.
Publications dans "Mastadenovirus" :
2 publications dans cette catégorie
Affiliations :
Universidade Feevale, Instituto de Ciências da Saúde, Laboratório de Microbiologia Molecular, Novo Hamburgo, Rio Grande do Sul, Brazil.
Publications dans "Mastadenovirus" :
With the advancement of molecular technology, fetal talipes equinovarus (TE) is believed to be not only associated with chromosome aneuploidy, but also related to chromosomal microdeletion and microdu...
This retrospectively study included 131 fetuses with TE identified by ultrasonography. Conventional karyotyping and SNP array analysis were performed for all the subjects. They were divided into isola...
Among the total of 131 fetuses, karyotype analysis found 12(9.2%) abnormal results, while SNP array found 27 (20.6%) cases. Trisomy 18 was detected most frequently among abnormal karyotypes. The detec...
Fetal TE is related to chromosomal microdeletion or microduplication. Prenatal diagnosis is recommended for fetuses with TE, and CMA testing is preferred. CMA can improve the detection rate of chromos...
Differential methylation (DM) is actively recruited in different types of fundamental and translational studies. Currently, microarray- and NGS-based approaches for methylation analysis are the most w...
To investigate the efficacy and outcomes of chromosomal microarray (CMA) in the cytogenomic evaluation of products of conception (POC)....
Over a 42-month period, 323 POC samples were tested by CMA. Results were assessed using variables including phenotype, gestational age, results from orthogonal testing, and follow-up parental analysis...
CMA identified cytogenetic abnormalities in 47.4% of first trimester losses and 10.9% of second and third trimester losses. Chromosomal microarray results specifically from 5 to 7-week losses showed s...
Our findings of specific types of genetic abnormalities and the respective frequencies by gestational age closely align with those of published karyotype studies, supporting the use of routine CMA tes...
Background Chromosomal microarray analysis (CMA) provides an opportunity to understand genetic causes of congenital heart disease (CHD). The methods for describing cardiac phenotypes in patients with ...
Emerging studies suggest that whole genome sequencing provides additional diagnostic yield of genomic variants when compared with chromosomal microarray analysis in the etiologic diagnosis of infants ...
This study aimed to evaluate the accuracy, efficacy, and incremental yield of whole genome sequencing in comparison with chromosomal microarray analysis for routine prenatal diagnosis....
In this prospective study, a total of 185 unselected singleton fetuses with ultrasound-detected structural anomalies were enrolled. In parallel, each sample was subjected to whole genome sequencing an...
Overall, genetic diagnoses using whole genome sequencing were obtained for 28 (15.1%) cases. Whole genome sequencing not only detected all these aneuploidies and copy number variations in the 20 (10.8...
Compared with chromosomal microarray analysis, whole genome sequencing increased the additional detection rate by 5.9% (11/185). Using whole genome sequencing, we detected not only aneuploidies and co...
The current study aimed to compare the characteristics of chromosome abnormalities detected by conventional G-banding karyotyping, chromosome microarray analysis (CMA), or fluorescence in situ hybridi...
From March 2019 to March 2021, 3710 amniocentesis samples were retrospectively collected from women who accepted prenatal diagnosis at 16 to 22 + 6 weeks of pregnancy. The pregnant women underwent kar...
In total, 3710 G-banding karyotype results and CMA results from invasive prenatal diagnosis were collected. Of these, 201 (5.41%) fetuses with an abnormal karyotype were observed. The CMA analysis sho...
Conventional G-banding karyotyping and CMA have their own advantages and limitations. A combination of karyotype analysis and CMA can increase the detection rate of chromosome abnormalities and make u...
Chromosomal microarray analysis (CMA) is considered a first-tier test for patients with developmental disabilities and congenital anomalies and is also routinely applied in prenatal diagnosis. The cur...
Autism spectrum disorder (ASD) is characterized by high heritability estimates and recurrence rates; its genetic underpinnings are very heterogeneous and include variable combinations of common and ra...
The aim of this study was to evaluate both diagnostic yield and clinical impact of aCGH in 329 ASD patients of Italian descent....
Pathogenic/likely pathogenic CNVs were identified in 50/329 (15.2%) patients, whereas 89/329 (27.1%) carry variants of uncertain significance. The 10 most enriched gene sets identified by Gene Ontolog...
This study confirms the satisfactory diagnostic yield of aCGH, underscoring its potential for better, more in-depth care of children with autism when genetic results are analyzed also with a focus on ...
Azoospermia consists of a significant proportion of infertility aetiology in males. Although known genetic abnormalities may explain roughly the third of infertility cases, the exact aetiology is stil...
This study was performed to assess the optimal resolution for prenatal testing by array comparative genomic hybridization (aCGH), aiming to balance between maximum diagnostic yield and minimal detecti...
This was a prospective study using data of 2,336 fetuses that underwent invasive prenatal diagnosis, and the samples were analyzed by aCGH. In total, six different aCGH platforms were studied; four di...
The diagnostic yield of copy number variants increased with increasing level of analysis. The detection rates of clinically significant chromosomal abnormalities were almost the same across our target...
It appears that the targeted array platform with 0.5 Mb backbone resolution and 0.05 Mb on targeted gene-rich regions is optimal for routine chromosomal microarray analysis use in prenatal diagnosis. ...