[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100552635":3},{"organization":4,"armGroups":7,"interventions":46,"overallOfficials":52,"centralContacts":56,"locations":66,"responsibleParty":83,"collaborators":85,"id":88,"slug":89,"hasResults":90,"nctId":91,"briefTitle":92,"officialTitle":92,"acronym":93,"eligibilityCriteria":94,"healthyVolunteers":95,"sex":96,"minAge":97,"maxAge":98,"enrollmentInfo":99,"targetDuration":10,"studyType":102,"phases":10,"briefSummary":103,"conditions":104,"keywords":107,"overallStatus":69,"whyStopped":10,"lastUpdateSubmitDate":118,"lastUpdatePostDateStruct":119,"startDateStruct":122,"completionDateStruct":124,"leadSponsor":126,"locationsCount":127},{"fullName":5,"class":6},"Assistance Publique - Hôpitaux de Paris","OTHER",[8,14,18,22,26,30,34,38,42],{"label":9,"type":10,"description":11,"interventionNames":12},"Workpackage 1, group 1",null,"Patients (children) with CHARGE syndrome",[13],"Genetic: Methylation analysis",{"label":15,"type":10,"description":16,"interventionNames":17},"Workpackage 1, group 2","Healthy negative controls (children) matched for age and sex",[13],{"label":19,"type":10,"description":20,"interventionNames":21},"Workpackage 1, group 3","Fetuses with CHARGE syndrome",[13],{"label":23,"type":10,"description":24,"interventionNames":25},"Workpackage 1, group 4","Fetuses with no genetic pathology",[13],{"label":27,"type":10,"description":28,"interventionNames":29},"Workpackage 2, group 5","Patients (children) with KABUKI syndrome",[13],{"label":31,"type":10,"description":32,"interventionNames":33},"Workpackage 2, group 6","Fetuses with KABUKI syndrome",[13],{"label":35,"type":10,"description":36,"interventionNames":37},"Workpackage 3, group 7","Fetuses with hydrolethalus syndrome",[13],{"label":39,"type":10,"description":40,"interventionNames":41},"Workpackage 3, group 8","Fetuses with Meckel\u002FOFD IV syndrome",[13],{"label":43,"type":10,"description":44,"interventionNames":45},"Workpackage 3, group 9","Fetuses with Fowler syndrome",[13],[47],{"type":48,"name":49,"description":50,"armGroupLabels":51,"otherNames":10},"GENETIC","Methylation analysis","Genomic DNA will be treated with bisulfite. 500 ng of processed DNA is then hybrized on an EPICv2 array Infinium methylation (Illumina, San Diego, CA, USA). This microarray enables the analysis of approximately 865 000 methylation sites at promoters, enhancers, CpG islands, intergenic and intragenic regions. It is the most widely used chip in the literature, including almost all of the EPIGENETIC SIGNATURES reported in human pathology.",[9,15,19,23,27,31,35,39,43],[53],{"name":54,"affiliation":5,"role":55},"Manon TESSIER, MD, PhD","STUDY_DIRECTOR",[57,62],{"name":58,"role":59,"phone":60,"phoneExt":10,"email":61},"Nicolas BOURGON, MD, PhD","CONTACT","+33 1 42 19 27 96","nicolas.bourgon@aphp.fr",{"name":63,"role":59,"phone":64,"phoneExt":10,"email":65},"Nelly BRIAND, PhD","0144381862","nelly.briand@aphp.fr",[67],{"facility":68,"status":69,"city":70,"state":10,"zip":71,"country":72,"countryCode":73,"cosmosGeoPoint":74,"geoPoint":79,"contacts":80},"Department of Genomic Medicine for Rare Diseases and the Multidisciplinary Center for Prenatal Diagnosis of the Necker-Enfants malades Hospital","RECRUITING","Paris","75015","France","FR",{"type":75,"coordinates":76},"Point",[77,78],2.3488,48.85341,{"lat":78,"lon":77},[81],{"name":58,"role":59,"phone":82,"phoneExt":10,"email":61},": +33 1 42 19 27 96",{"type":84,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR",[86],{"name":87,"class":6},"URC-CIC Paris Descartes Necker Cochin","100552635","characterization-and-contribution-of-genome-wide-dna-methylation-dna-methylation-episignatures-in-rare-diseases-with-prenatal-onset-100552635",false,"NCT06475651","Characterization and Contribution of Genome-wide DNA Methylation (DNA Methylation Episignatures) in Rare Diseases With Prenatal Onset","FOETEPISIGN","Inclusion Criteria:\n\n* Patient Inclusion Criteria:\n\n  * Fetuses with a postmortem examination as part of the etiological diagnosis of developmental abnormality within the Genomic Medicine of Rare Diseases department of the Necker Children's Hospital, and whose DNA extracted from lung and amniotic fluid is available\n  * OR a child cared for in the Genomic Medicine for Rare Diseases department of the Necker Children's Hospital, and whose DNA extracted from whole blood is available\n  * with pathogenic or probably pathogenic variation in a gene following CHD7, KMT2D, HYLS1, TCTN3 or FLVCR2\n  * whose parents have consented to molecular genetic testing as part of diagnosis and research\n* Negative Controls :\n\n  * Fetuses with a postmortem examination as part of the etiological diagnosis of developmental abnormality within the Genomic Medicine of Rare Diseases department of the Necker Children's Hospital, and whose DNA extracted from lung and amniotic fluid are available\n  * OR a child cared for in the Genomic Medicine for Rare Diseases department of the Necker Children's Hospital, and whose DNA extracted from whole blood is available\n  * does not have pathogenic or probably pathogenic variation in a gene following CHD7, KMT2D, HYLS1, TCTN3 or FLVCR2\n  * whose parents have consented to molecular genetic testing as part of diagnosis and research\n* For everyone:\n\n  • For living participants: Non-objection by holders of parental authority to the reuse of clinical data and biological samples collected and stored in the context of care (consent of care).\n\n  • For deceased participants:\n* Consent of the holders of parental authority to the use of the samples kept for research purposes, signed as part of the treatment\n* No mention of opposition to the reuse of clinical data from the treatment in the patient's medical record\n\nExclusion Criteria:\n\n* Refusal of postmortem examination in case of fetal loss\n* Parents' refusal of molecular investigations",true,"ALL","0 Years","18 Years",{"count":100,"type":101},63,"ESTIMATED","OBSERVATIONAL","It is necessary to define reference DNA Methylation Episignatures from fetal DNA. The hypotheses are:\n\n* It is possible to define reference DNA Methylation Episignatures from fetal DNA extracted from amniotic fluid or frozen tissues collected during the postmortem examination\n* Fetal DNA Methylation Episignatures may be different to postanal DNA Methylation Episignatures defined on DNA extracted from blood",[105,106],"Rare Fetal Genetic Diseases","Congenital Malformation",[108,109,110,111,112,113,114,115,116,117],"Congenital malformation","DNA methylation abnormalities","Episignature","CHD7 gene","KMT2D gene","HYLS1 gene","TCTN3 gene","FLVCR2 gene","CHARGE syndrome","KABUKI syndrome","2026-03-24",{"date":120,"type":121},"2026-03-27","ACTUAL",{"date":123,"type":121},"2026-02-26",{"date":125,"type":101},"2026-08-26",{"name":5,"class":6},1]