questionsmedicales.fr
Phénomènes génétiques
Variation génétique
Mutation
Aberrations des chromosomes
Aberrations des chromosomes : Questions médicales fréquentes
Termes MeSH sélectionnés :
{
"@context": "https://schema.org",
"@graph": [
{
"@type": "MedicalWebPage",
"name": "Aberrations des chromosomes : Questions médicales les plus fréquentes",
"headline": "Aberrations des chromosomes : Comprendre les symptômes, diagnostics et traitements",
"description": "Guide complet et accessible sur les Aberrations des chromosomes : explications, diagnostics, traitements et prévention. Information médicale validée destinée aux patients.",
"datePublished": "2024-05-10",
"dateModified": "2025-05-05",
"inLanguage": "fr",
"medicalAudience": [
{
"@type": "MedicalAudience",
"name": "Grand public",
"audienceType": "Patient",
"healthCondition": {
"@type": "MedicalCondition",
"name": "Aberrations des chromosomes"
},
"suggestedMinAge": 18,
"suggestedGender": "unisex"
},
{
"@type": "MedicalAudience",
"name": "Médecins",
"audienceType": "Physician",
"geographicArea": {
"@type": "AdministrativeArea",
"name": "France"
}
},
{
"@type": "MedicalAudience",
"name": "Chercheurs",
"audienceType": "Researcher",
"geographicArea": {
"@type": "AdministrativeArea",
"name": "International"
}
}
],
"reviewedBy": {
"@type": "Person",
"name": "Dr Olivier Menir",
"jobTitle": "Expert en Médecine",
"description": "Expert en Médecine, Optimisation des Parcours de Soins et Révision Médicale",
"url": "/static/pages/docteur-olivier-menir.html",
"alumniOf": {
"@type": "EducationalOrganization",
"name": "Université Paris Descartes"
}
},
"isPartOf": {
"@type": "MedicalWebPage",
"name": "Mutation",
"url": "https://questionsmedicales.fr/mesh/D009154",
"about": {
"@type": "MedicalCondition",
"name": "Mutation",
"code": {
"@type": "MedicalCode",
"code": "D009154",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590"
}
}
},
"hasPart": [
{
"@type": "MedicalWebPage",
"name": "Caryotype anormal",
"alternateName": "Abnormal Karyotype",
"url": "https://questionsmedicales.fr/mesh/D059786",
"about": {
"@type": "MedicalCondition",
"name": "Caryotype anormal",
"code": {
"@type": "MedicalCode",
"code": "D059786",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.024"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Chimérisme",
"alternateName": "Chimerism",
"url": "https://questionsmedicales.fr/mesh/D046528",
"about": {
"@type": "MedicalCondition",
"name": "Chimérisme",
"code": {
"@type": "MedicalCode",
"code": "D046528",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.125"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Cassure de chromosome",
"alternateName": "Chromosome Breakage",
"url": "https://questionsmedicales.fr/mesh/D019457",
"about": {
"@type": "MedicalCondition",
"name": "Cassure de chromosome",
"code": {
"@type": "MedicalCode",
"code": "D019457",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.175"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Chromothripsis",
"alternateName": "Chromothripsis",
"url": "https://questionsmedicales.fr/mesh/D000072837",
"about": {
"@type": "MedicalCondition",
"name": "Chromothripsis",
"code": {
"@type": "MedicalCode",
"code": "D000072837",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.310"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Isochromosomes",
"alternateName": "Isochromosomes",
"url": "https://questionsmedicales.fr/mesh/D018404",
"about": {
"@type": "MedicalCondition",
"name": "Isochromosomes",
"code": {
"@type": "MedicalCode",
"code": "D018404",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.430"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Micronoyaux à chromosomes défectueux",
"alternateName": "Micronuclei, Chromosome-Defective",
"url": "https://questionsmedicales.fr/mesh/D048629",
"about": {
"@type": "MedicalCondition",
"name": "Micronoyaux à chromosomes défectueux",
"code": {
"@type": "MedicalCode",
"code": "D048629",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.570"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Mosaïcisme",
"alternateName": "Mosaicism",
"url": "https://questionsmedicales.fr/mesh/D009030",
"about": {
"@type": "MedicalCondition",
"name": "Mosaïcisme",
"code": {
"@type": "MedicalCode",
"code": "D009030",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.595"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Chromosomes en anneau",
"alternateName": "Ring Chromosomes",
"url": "https://questionsmedicales.fr/mesh/D012303",
"about": {
"@type": "MedicalCondition",
"name": "Chromosomes en anneau",
"code": {
"@type": "MedicalCode",
"code": "D012303",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.760"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Aberrations des chromosomes sexuels",
"alternateName": "Sex Chromosome Aberrations",
"url": "https://questionsmedicales.fr/mesh/D012729",
"about": {
"@type": "MedicalCondition",
"name": "Aberrations des chromosomes sexuels",
"code": {
"@type": "MedicalCode",
"code": "D012729",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.815"
}
},
"hasPart": [
{
"@type": "MedicalWebPage",
"name": "Caryotype XYY",
"alternateName": "XYY Karyotype",
"url": "https://questionsmedicales.fr/mesh/D014997",
"about": {
"@type": "MedicalCondition",
"name": "Caryotype XYY",
"code": {
"@type": "MedicalCode",
"code": "D014997",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.815.970"
}
}
}
]
},
{
"@type": "MedicalWebPage",
"name": "Chromosome Philadelphie",
"alternateName": "Philadelphia Chromosome",
"url": "https://questionsmedicales.fr/mesh/D010677",
"about": {
"@type": "MedicalCondition",
"name": "Chromosome Philadelphie",
"code": {
"@type": "MedicalCode",
"code": "D010677",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.870.680"
}
}
},
{
"@type": "MedicalWebPage",
"name": "Disomie uniparentale",
"alternateName": "Uniparental Disomy",
"url": "https://questionsmedicales.fr/mesh/D024182",
"about": {
"@type": "MedicalCondition",
"name": "Disomie uniparentale",
"code": {
"@type": "MedicalCode",
"code": "D024182",
"codingSystem": "MeSH"
},
"identifier": {
"@type": "PropertyValue",
"propertyID": "MeSH Tree",
"value": "G05.365.590.175.935"
}
}
}
],
"about": {
"@type": "MedicalCondition",
"name": "Aberrations des chromosomes",
"alternateName": "Chromosome Aberrations",
"code": {
"@type": "MedicalCode",
"code": "D002869",
"codingSystem": "MeSH"
}
},
"author": [
{
"@type": "Person",
"name": "Kari Hemminki",
"url": "https://questionsmedicales.fr/author/Kari%20Hemminki",
"affiliation": {
"@type": "Organization",
"name": "Faculty of Medicine and Biomedical Center in Pilsen, Charles University, 32300 Pilsen, Czech Republic."
}
},
{
"@type": "Person",
"name": "Yasmeen Niazi",
"url": "https://questionsmedicales.fr/author/Yasmeen%20Niazi",
"affiliation": {
"@type": "Organization",
"name": "Hopp Children's Cancer Center (KiTZ), Heidelberg, Germany."
}
},
{
"@type": "Person",
"name": "Ludmila Vodickova",
"url": "https://questionsmedicales.fr/author/Ludmila%20Vodickova",
"affiliation": {
"@type": "Organization",
"name": "Faculty of Medicine and Biomedical Center in Pilsen, Charles University, 32300 Pilsen, Czech Republic."
}
},
{
"@type": "Person",
"name": "Pavel Vodicka",
"url": "https://questionsmedicales.fr/author/Pavel%20Vodicka",
"affiliation": {
"@type": "Organization",
"name": "Faculty of Medicine and Biomedical Center in Pilsen, Charles University, 32300 Pilsen, Czech Republic."
}
},
{
"@type": "Person",
"name": "Asta Försti",
"url": "https://questionsmedicales.fr/author/Asta%20F%C3%B6rsti",
"affiliation": {
"@type": "Organization",
"name": "Hopp Children's Cancer Center (KiTZ), Heidelberg, Germany."
}
}
],
"citation": [
{
"@type": "ScholarlyArticle",
"name": "Assessing trial representativeness using serious adverse events: an observational analysis using aggregate and individual-level data from clinical trials and routine healthcare data.",
"datePublished": "2022-10-28",
"url": "https://questionsmedicales.fr/article/36303169",
"identifier": {
"@type": "PropertyValue",
"propertyID": "DOI",
"value": "10.1186/s12916-022-02594-9"
}
},
{
"@type": "ScholarlyArticle",
"name": "Genome-Wide Analysis of Yeast Metabolic Cycle through Metabolic Network Models Reveals Superiority of Integrated ATAC-seq Data over RNA-seq Data.",
"datePublished": "2022-06-13",
"url": "https://questionsmedicales.fr/article/35695574",
"identifier": {
"@type": "PropertyValue",
"propertyID": "DOI",
"value": "10.1128/msystems.01347-21"
}
},
{
"@type": "ScholarlyArticle",
"name": "Comparison of real data and simulated data analysis of a stopping rule based on the standard error of measurement in computerized adaptive testing for medical examinations in Korea: a psychometric study.",
"datePublished": "2024-07-09",
"url": "https://questionsmedicales.fr/article/38977033",
"identifier": {
"@type": "PropertyValue",
"propertyID": "DOI",
"value": "10.3352/jeehp.2024.21.18"
}
},
{
"@type": "ScholarlyArticle",
"name": "Integrating real-world data to assess cardiac ablation device outcomes in a multicenter study using the OMOP common data model for regulatory decisions: implementation and evaluation.",
"datePublished": "2023-01-10",
"url": "https://questionsmedicales.fr/article/36632328",
"identifier": {
"@type": "PropertyValue",
"propertyID": "DOI",
"value": "10.1093/jamiaopen/ooac108"
}
},
{
"@type": "ScholarlyArticle",
"name": "Acknowledging and citing core facilities: Key contributions to data lifecycle should be recognised in the scientific literature: Key contributions to data lifecycle should be recognised in the scientific literature.",
"datePublished": "2022-08-23",
"url": "https://questionsmedicales.fr/article/35997112",
"identifier": {
"@type": "PropertyValue",
"propertyID": "DOI",
"value": "10.15252/embr.202255734"
}
}
],
"breadcrumb": {
"@type": "BreadcrumbList",
"itemListElement": [
{
"@type": "ListItem",
"position": 1,
"name": "questionsmedicales.fr",
"item": "https://questionsmedicales.fr"
},
{
"@type": "ListItem",
"position": 2,
"name": "Phénomènes génétiques",
"item": "https://questionsmedicales.fr/mesh/D055614"
},
{
"@type": "ListItem",
"position": 3,
"name": "Variation génétique",
"item": "https://questionsmedicales.fr/mesh/D014644"
},
{
"@type": "ListItem",
"position": 4,
"name": "Mutation",
"item": "https://questionsmedicales.fr/mesh/D009154"
},
{
"@type": "ListItem",
"position": 5,
"name": "Aberrations des chromosomes",
"item": "https://questionsmedicales.fr/mesh/D002869"
}
]
}
},
{
"@type": "MedicalWebPage",
"name": "Article complet : Aberrations des chromosomes - Questions et réponses",
"headline": "Questions et réponses médicales fréquentes sur Aberrations des chromosomes",
"description": "Une compilation de questions et réponses structurées, validées par des experts médicaux.",
"datePublished": "2025-05-15",
"inLanguage": "fr",
"hasPart": [
{
"@type": "MedicalWebPage",
"name": "Diagnostic",
"headline": "Diagnostic sur Aberrations des chromosomes",
"description": "Comment diagnostique-t-on une aberration chromosomique ?\nQuels tests sont utilisés pour détecter les aberrations chromosomiques ?\nLes échographies peuvent-elles détecter des anomalies chromosomiques ?\nQuel rôle joue le conseil génétique dans le diagnostic ?\nLes tests sanguins peuvent-ils révéler des aberrations chromosomiques ?",
"url": "https://questionsmedicales.fr/mesh/D002869?mesh_terms=Data+Science&page=1000#section-diagnostic"
},
{
"@type": "MedicalWebPage",
"name": "Symptômes",
"headline": "Symptômes sur Aberrations des chromosomes",
"description": "Quels sont les symptômes des aberrations chromosomiques ?\nLes aberrations chromosomiques causent-elles des troubles mentaux ?\nPeut-on avoir des symptômes sans aberration chromosomique visible ?\nLes symptômes varient-ils selon le type d'aberration ?\nLes anomalies chromosomiques peuvent-elles affecter la fertilité ?",
"url": "https://questionsmedicales.fr/mesh/D002869?mesh_terms=Data+Science&page=1000#section-symptômes"
},
{
"@type": "MedicalWebPage",
"name": "Prévention",
"headline": "Prévention sur Aberrations des chromosomes",
"description": "Peut-on prévenir les aberrations chromosomiques ?\nLe dépistage prénatal peut-il réduire les risques ?\nLes habitudes de vie influencent-elles les aberrations chromosomiques ?\nLes vaccinations peuvent-elles prévenir des anomalies ?\nLe suivi médical avant la grossesse est-il important ?",
"url": "https://questionsmedicales.fr/mesh/D002869?mesh_terms=Data+Science&page=1000#section-prévention"
},
{
"@type": "MedicalWebPage",
"name": "Traitements",
"headline": "Traitements sur Aberrations des chromosomes",
"description": "Quels traitements existent pour les aberrations chromosomiques ?\nLa thérapie génique est-elle une option pour ces anomalies ?\nLes médicaments peuvent-ils aider à gérer les symptômes ?\nLe suivi médical est-il important pour ces patients ?\nLes interventions précoces sont-elles bénéfiques ?",
"url": "https://questionsmedicales.fr/mesh/D002869?mesh_terms=Data+Science&page=1000#section-traitements"
},
{
"@type": "MedicalWebPage",
"name": "Complications",
"headline": "Complications sur Aberrations des chromosomes",
"description": "Quelles complications peuvent survenir avec des aberrations chromosomiques ?\nLes aberrations chromosomiques augmentent-elles le risque de cancer ?\nLes problèmes cardiaques sont-ils fréquents avec ces anomalies ?\nLes troubles du comportement sont-ils liés aux aberrations chromosomiques ?\nLes complications peuvent-elles affecter la qualité de vie ?",
"url": "https://questionsmedicales.fr/mesh/D002869?mesh_terms=Data+Science&page=1000#section-complications"
},
{
"@type": "MedicalWebPage",
"name": "Facteurs de risque",
"headline": "Facteurs de risque sur Aberrations des chromosomes",
"description": "Quels sont les facteurs de risque d'aberrations chromosomiques ?\nL'exposition à des substances toxiques augmente-t-elle le risque ?\nLes antécédents familiaux jouent-ils un rôle ?\nLe stress peut-il influencer le risque d'anomalies ?\nLes infections pendant la grossesse sont-elles un facteur de risque ?",
"url": "https://questionsmedicales.fr/mesh/D002869?mesh_terms=Data+Science&page=1000#section-facteurs de risque"
}
]
},
{
"@type": "FAQPage",
"mainEntity": [
{
"@type": "Question",
"name": "Comment diagnostique-t-on une aberration chromosomique ?",
"position": 1,
"acceptedAnswer": {
"@type": "Answer",
"text": "Le diagnostic se fait par analyse cytogénétique, comme le caryotype."
}
},
{
"@type": "Question",
"name": "Quels tests sont utilisés pour détecter les aberrations chromosomiques ?",
"position": 2,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les tests incluent le caryotype, l'hybridation in situ et le séquençage génétique."
}
},
{
"@type": "Question",
"name": "Les échographies peuvent-elles détecter des anomalies chromosomiques ?",
"position": 3,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, certaines anomalies peuvent être suspectées par échographie prénatale."
}
},
{
"@type": "Question",
"name": "Quel rôle joue le conseil génétique dans le diagnostic ?",
"position": 4,
"acceptedAnswer": {
"@type": "Answer",
"text": "Le conseil génétique aide à évaluer le risque et à interpréter les résultats des tests."
}
},
{
"@type": "Question",
"name": "Les tests sanguins peuvent-ils révéler des aberrations chromosomiques ?",
"position": 5,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, des tests sanguins peuvent détecter des anomalies chromosomiques spécifiques."
}
},
{
"@type": "Question",
"name": "Quels sont les symptômes des aberrations chromosomiques ?",
"position": 6,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les symptômes varient, incluant des malformations congénitales et des retards de développement."
}
},
{
"@type": "Question",
"name": "Les aberrations chromosomiques causent-elles des troubles mentaux ?",
"position": 7,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, certaines aberrations peuvent être associées à des troubles du développement intellectuel."
}
},
{
"@type": "Question",
"name": "Peut-on avoir des symptômes sans aberration chromosomique visible ?",
"position": 8,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, certaines anomalies peuvent ne pas être visibles mais entraîner des symptômes."
}
},
{
"@type": "Question",
"name": "Les symptômes varient-ils selon le type d'aberration ?",
"position": 9,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, les symptômes dépendent du type d'aberration et des gènes affectés."
}
},
{
"@type": "Question",
"name": "Les anomalies chromosomiques peuvent-elles affecter la fertilité ?",
"position": 10,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, certaines aberrations peuvent entraîner des problèmes de fertilité ou des fausses couches."
}
},
{
"@type": "Question",
"name": "Peut-on prévenir les aberrations chromosomiques ?",
"position": 11,
"acceptedAnswer": {
"@type": "Answer",
"text": "Certaines aberrations ne peuvent pas être prévenues, mais le conseil génétique aide à évaluer les risques."
}
},
{
"@type": "Question",
"name": "Le dépistage prénatal peut-il réduire les risques ?",
"position": 12,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, le dépistage prénatal permet d'identifier les risques d'anomalies chromosomiques."
}
},
{
"@type": "Question",
"name": "Les habitudes de vie influencent-elles les aberrations chromosomiques ?",
"position": 13,
"acceptedAnswer": {
"@type": "Answer",
"text": "Certaines habitudes, comme l'alcool et le tabac, peuvent augmenter le risque d'anomalies."
}
},
{
"@type": "Question",
"name": "Les vaccinations peuvent-elles prévenir des anomalies ?",
"position": 14,
"acceptedAnswer": {
"@type": "Answer",
"text": "Certaines vaccinations peuvent prévenir des infections qui pourraient causer des anomalies."
}
},
{
"@type": "Question",
"name": "Le suivi médical avant la grossesse est-il important ?",
"position": 15,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, un suivi médical peut aider à identifier et gérer les risques avant la grossesse."
}
},
{
"@type": "Question",
"name": "Quels traitements existent pour les aberrations chromosomiques ?",
"position": 16,
"acceptedAnswer": {
"@type": "Answer",
"text": "Le traitement dépend des symptômes, incluant thérapies, chirurgie ou soutien éducatif."
}
},
{
"@type": "Question",
"name": "La thérapie génique est-elle une option pour ces anomalies ?",
"position": 17,
"acceptedAnswer": {
"@type": "Answer",
"text": "La thérapie génique est en recherche, mais pas encore largement disponible pour ces anomalies."
}
},
{
"@type": "Question",
"name": "Les médicaments peuvent-ils aider à gérer les symptômes ?",
"position": 18,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, des médicaments peuvent être prescrits pour gérer certains symptômes associés."
}
},
{
"@type": "Question",
"name": "Le suivi médical est-il important pour ces patients ?",
"position": 19,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, un suivi régulier est crucial pour surveiller les complications et ajuster les traitements."
}
},
{
"@type": "Question",
"name": "Les interventions précoces sont-elles bénéfiques ?",
"position": 20,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, les interventions précoces peuvent améliorer le développement et la qualité de vie."
}
},
{
"@type": "Question",
"name": "Quelles complications peuvent survenir avec des aberrations chromosomiques ?",
"position": 21,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les complications incluent des malformations, des troubles de la croissance et des problèmes de santé."
}
},
{
"@type": "Question",
"name": "Les aberrations chromosomiques augmentent-elles le risque de cancer ?",
"position": 22,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, certaines aberrations chromosomiques sont associées à un risque accru de cancer."
}
},
{
"@type": "Question",
"name": "Les problèmes cardiaques sont-ils fréquents avec ces anomalies ?",
"position": 23,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, certaines aberrations chromosomiques peuvent entraîner des malformations cardiaques."
}
},
{
"@type": "Question",
"name": "Les troubles du comportement sont-ils liés aux aberrations chromosomiques ?",
"position": 24,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, des troubles du comportement peuvent être associés à certaines anomalies chromosomiques."
}
},
{
"@type": "Question",
"name": "Les complications peuvent-elles affecter la qualité de vie ?",
"position": 25,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, les complications peuvent significativement impacter la qualité de vie des patients."
}
},
{
"@type": "Question",
"name": "Quels sont les facteurs de risque d'aberrations chromosomiques ?",
"position": 26,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les facteurs incluent l'âge maternel avancé, des antécédents familiaux et des expositions environnementales."
}
},
{
"@type": "Question",
"name": "L'exposition à des substances toxiques augmente-t-elle le risque ?",
"position": 27,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, l'exposition à des substances toxiques peut augmenter le risque d'anomalies chromosomiques."
}
},
{
"@type": "Question",
"name": "Les antécédents familiaux jouent-ils un rôle ?",
"position": 28,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, des antécédents familiaux d'anomalies chromosomiques augmentent le risque."
}
},
{
"@type": "Question",
"name": "Le stress peut-il influencer le risque d'anomalies ?",
"position": 29,
"acceptedAnswer": {
"@type": "Answer",
"text": "Certaines études suggèrent que le stress peut avoir un impact sur le risque d'anomalies chromosomiques."
}
},
{
"@type": "Question",
"name": "Les infections pendant la grossesse sont-elles un facteur de risque ?",
"position": 30,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, certaines infections pendant la grossesse peuvent augmenter le risque d'anomalies chromosomiques."
}
}
]
}
]
}
The applicability of randomised controlled trials of pharmacological agents to older people with frailty/multimorbidity is often uncertain, due to concerns that trials are not representative. However,...
This was an observational analysis of individual (125 trials, n=122,069) and aggregate-level drug trial data (483 trials, n=636,267) for 21 index conditions compared to population-based routine health...
For 12/21 index conditions, the pooled observed/expected SAE ratio was <1, indicating fewer SAEs in trial participants than in routine care. A further 6/21 had point estimates <1 but the 95% CI includ...
Trial participants experience fewer SAEs than expected based on age/sex/condition hospitalisation and death rates in routine care, confirming the predicted lack of representativeness. This difference ...
Saccharomyces cerevisiae undergoes robust oscillations to regulate its physiology for adaptation and survival under nutrient-limited conditions. Environmental cues can induce rhythmic metabolic altera...
This study aimed to compare and evaluate the efficiency and accuracy of computerized adaptive testing (CAT) under two stopping rules (SEM 0.3 and 0.25) using both real and simulated data in medical ex...
This study employed post-hoc simulation and real data analysis to explore the optimal stopping rule for CAT in medical examinations. The real data were obtained from the responses of 3rd-year medical ...
Both SEM 0.25 and SEM 0.30 provided a good balance between accuracy and efficiency in CAT. The real data showed minimal differences in pass/fail outcomes between the 2 SEM conditions, with a high corr...
The findings suggest that both SEM 0.25 and 0.30 are effective termination criteria in the context of the Rasch model, balancing accuracy and efficiency in CAT....
The objective of this study is to describe application of the Observational Medical Outcomes Partnership (OMOP) common data model (CDM) to support medical device real-world evaluation in a National Ev...
Core facilities play a central role in the life sciences by generating data and ensuring quality standards. Their contributions to research should be appropriately acknowledged or cited in research pa...
Understanding race and ethnicity (RE) differentials improves health outcomes. However, RE data are consistently missing from electronic laboratory reports, the primary source of COVID-19 case metrics....
This descriptive epidemiology cross-sectional study linked the NYS Electronic Clinical Laboratory Reporting System (ECLRS) with NYS Immunization Information System (NYSIIS) to address the missing RE d...
There were 4,212,741 COVID-19 cases with 39% (1,624,818) missing RE data in ECLRS; missing RE data declined to 17% (726,023) after matching with NYSIIS. For those aged 65 years or older (after matchin...
Matching case data with vaccine registries reduce missing RE data for COVID-19 cases. Disparity was lower in vaccinated than in unvaccinated individuals indicating that vaccination mitigated RE dispar...
The integration of health and activity data from various wearable devices into research studies presents technical and operational challenges. The Awesome Data Acquisition Method (ADAM) is a versatile...
The pernicious nature of low-quality sequencing data warrants improvement in the bioinformatics workflow for profiling microbial diversity. The conventional merging approach, which drops a copious amo...
Polypharmacy is commonly observed in atrial fibrillation (AF) and is associated with poorer clinical outcomes. Our study aimed to elucidate the polypharmacy prevalence, its associated risk factors, an...
This study included 451,368 subjects without prior history of AF (median age, 54 [interquartile range, 48.0-63.0] years; 207,748 [46.0%] female) from the Korea National Health Insurance Service-Health...
Based on up to 7.7 (6.8-8.3) years of follow-up and 768,306 person-years, there were 12,241 cases of new-onset AF identified. Among patients with new-onset AF (40.0% females, median age 63.0 [54.0-70....
In our investigation using data from a nationwide database, polypharmacy was widespread in new-onset AF population and was related to major bleeding events. However, polypharmacy does not serve as an ...
Railway suicide has profound implications for the victims and their family, and affects train drivers, railway personnel, emergency services and witnesses. To inform a multilevel prevention strategy, ...
Data from Statistics Netherlands of all suicides between 2017 and 2021 (n = 9.241) of whom 986 died by railway suicide and interview data from a psychosocial autopsy of railway suicide decedents (n = ...
The strongest predictors of railway suicide compared to other suicide methods were young age (< 30 years old), native Dutch, a high educational level, living in a multi-person household (especially li...
based on our findings we propose and discuss several recommendations to prevent railway suicide. We must continue to invest in a safe railway environment by training personnel and installing barriers....