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Bactéries
Proteobacteria
Betaproteobacteria
Burkholderiales
Alcaligenaceae
Alcaligenaceae : Questions médicales fréquentes
Termes MeSH sélectionnés :
Diagnostic
5
Infections bactériennes
Culture bactérienne
Antibiotiques
Analyse génétique
Culture bactérienne
Milieu de culture
Symptômes
Infections bactériennes
PCR
Détection bactérienne
Symptômes
5
Symptômes
Infections bactériennes
Douleur
Infections bactériennes
Variabilité des symptômes
Infections bactériennes
Infections asymptomatiques
Portage bactérien
Gravité des symptômes
Immunodépression
Prévention
5
Prévention des infections
Hygiène
Vaccination
Prévention des infections
Contrôle des infections
Soins hospitaliers
Immunodépression
Prévention des infections
Lavage des mains
Prévention des infections
Traitements
5
Antibiotiques
Traitement des infections
Résistance aux antibiotiques
Sensibilité bactérienne
Antibiotiques oraux
Traitement des infections
Hospitalisation
Infections bactériennes
Thérapies ciblées
Traitement des infections
Complications
5
Infections mortelles
Risque
Complications à long terme
Problèmes respiratoires
Hospitalisation prolongée
Infections bactériennes
Comorbidités
Complications
Facteurs de risque
5
Facteurs de risque
Immunodépression
Diabète
Infections opportunistes
Personnes âgées
Vulnérabilité
Soins intensifs
Infections nosocomiales
Immunosuppression
Facteurs de risque
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"name": "Les infections par Alcaligenaceae nécessitent-elles une hospitalisation ?",
"position": 19,
"acceptedAnswer": {
"@type": "Answer",
"text": "Cela dépend de la gravité de l'infection et de l'état du patient, souvent oui."
}
},
{
"@type": "Question",
"name": "Y a-t-il des traitements alternatifs pour Alcaligenaceae ?",
"position": 20,
"acceptedAnswer": {
"@type": "Answer",
"text": "Des traitements alternatifs peuvent inclure des thérapies ciblées, mais sont moins courants."
}
},
{
"@type": "Question",
"name": "Quelles complications peuvent survenir avec Alcaligenaceae ?",
"position": 21,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les complications incluent des infections systémiques, septicémie et défaillance d'organes."
}
},
{
"@type": "Question",
"name": "Les infections par Alcaligenaceae peuvent-elles être mortelles ?",
"position": 22,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, surtout chez les patients à risque, les infections peuvent être graves et mortelles."
}
},
{
"@type": "Question",
"name": "Y a-t-il des complications à long terme ?",
"position": 23,
"acceptedAnswer": {
"@type": "Answer",
"text": "Des complications à long terme peuvent inclure des problèmes respiratoires ou neurologiques."
}
},
{
"@type": "Question",
"name": "Les infections par Alcaligenaceae entraînent-elles des hospitalisations prolongées ?",
"position": 24,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, les infections graves peuvent nécessiter des hospitalisations prolongées pour traitement."
}
},
{
"@type": "Question",
"name": "Les complications sont-elles fréquentes ?",
"position": 25,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les complications sont plus fréquentes chez les patients immunodéprimés ou avec comorbidités."
}
},
{
"@type": "Question",
"name": "Quels sont les facteurs de risque d'infection par Alcaligenaceae ?",
"position": 26,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les facteurs incluent l'immunodépression, les interventions chirurgicales et l'hospitalisation prolongée."
}
},
{
"@type": "Question",
"name": "Les patients diabétiques sont-ils à risque ?",
"position": 27,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, les patients diabétiques ont un risque accru d'infections opportunistes, y compris Alcaligenaceae."
}
},
{
"@type": "Question",
"name": "Les personnes âgées sont-elles plus vulnérables ?",
"position": 28,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, les personnes âgées sont souvent plus vulnérables aux infections bactériennes."
}
},
{
"@type": "Question",
"name": "Les soins intensifs augmentent-ils le risque d'infection ?",
"position": 29,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, les patients en soins intensifs sont à risque accru d'infections nosocomiales."
}
},
{
"@type": "Question",
"name": "Les traitements immunosuppresseurs sont-ils un facteur de risque ?",
"position": 30,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, les traitements immunosuppresseurs augmentent le risque d'infections par Alcaligenaceae."
}
}
]
}
]
}
Expert en Médecine, Optimisation des Parcours de Soins et Révision Médicale
Validation scientifique effectuée le 30/03/2025
Contenu vérifié selon les dernières recommandations médicales
1 publication dans cette catégorie
Affiliations :
Biotechnology Department, Faculty of Agriculture, Bu-Ali Sina University, Hamedan, Islamic Republic of Iran.
Publications dans "Alcaligenaceae" :
1 publication dans cette catégorie
Affiliations :
Biotechnology Department, Faculty of Agriculture, Bu-Ali Sina University, Hamedan, Islamic Republic of Iran. snazeri@basu.ac.ir.
Publications dans "Alcaligenaceae" :
1 publication dans cette catégorie
Affiliations :
Department of Bioprocess Technology, Faculty of Biotechnology and Biomolecular Sciences, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor, Malaysia.
Publications dans "Alcaligenaceae" :
1 publication dans cette catégorie
Affiliations :
Department of Bioprocess Technology, Faculty of Biotechnology and Biomolecular Sciences, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor, Malaysia; Laboratory of Biopolymer and Derivatives, Institute of Tropical Forestry and Forest Products (INTROP), Universiti Putra Malaysia, 43400 UPM Serdang, Selangor, Malaysia. Electronic address: yatiramli@upm.edu.my.
Publications dans "Alcaligenaceae" :
1 publication dans cette catégorie
Affiliations :
Department of Bioprocess Technology, Faculty of Biotechnology and Biomolecular Sciences, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor, Malaysia.
Publications dans "Alcaligenaceae" :
1 publication dans cette catégorie
Affiliations :
Department of Biological Functions Engineering, Graduate School of Life Science and Systems Engineering, Kyushu Institute of Technology, 2-4 Hibikino, Wakamatsu-ku, Fukuoka 808-0196, Japan.
Publications dans "Alcaligenaceae" :
1 publication dans cette catégorie
Affiliations :
Department of Bioprocess Technology, Faculty of Biotechnology and Biomolecular Sciences, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor, Malaysia.
Publications dans "Alcaligenaceae" :
1 publication dans cette catégorie
Affiliations :
Department of Biological Functions Engineering, Graduate School of Life Science and Systems Engineering, Kyushu Institute of Technology, 2-4 Hibikino, Wakamatsu-ku, Fukuoka 808-0196, Japan.
Publications dans "Alcaligenaceae" :
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. ...