[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"neurogenetic-diseases\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:neurogenetic-diseases":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,48],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":20,"enrollmentInfo":21,"targetDuration":4,"studyType":24,"phases":25,"briefSummary":27,"conditions":28,"keywords":30,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":5},"100644164","advancing-neurogenetic-diagnoses-through-long-read-sequencing-100644164",false,"NCT07665554","Advancing Neurogenetic Diagnoses Through Long-Read Sequencing","NRGEN-NGS3 : Advancing Neurogenetic Diagnoses Through Long-Read Sequencing","NRGEN-NGS3","Inclusion Criteria:\n\n* All participants :\n\n  * Participants affiliated with or beneficiaries of a social security scheme\n  * Participants who speak French\n  * Participants aged ≥ 6 and ≤ 60 years\n* For patients requiring a new sample:\n\n  * Free and informed consent, signed by the parents or the holder of parental authority for patients under the age of 18\n  * Free and informed consent, signed by the patient's representative for adults under guardianship\n  * Free and informed consent, signed by the adult patient\n* For diagnosed patients :\n\n  • DeoxyriboNucleic Acid (DNA) sample from a subject carrying a nucleotide repeat expansion in one of the selected genes.\n  * DNA available in sufficient quantity (5-10 µg) or patient agreeing to a blood draw from which DNA will be extracted.\n  * DNA extraction methods known and validated by the steering committee (see paragraph 7).\n* For participants from undiagnosed families :\n\n  o Index cases:\n\n  • Patient affected by a neurological disease candidate for these repeats, for which genomic data did not reveal mutations or expansions in known genes.\n  * Patient whose DNA is already available and whose extraction method is known and validated by the steering committee or patient whose DNA is not available but who agrees to a blood draw.\n  * Patient willing to undergo a skin biopsy if not previously obtained.\n  * Patient with no family members affected by any of the neurological diseases candidate for these repeats, i.e., genomic data do not reveal mutations or expansions in known genes.\n  * Patient from a family in which at least one affected and one unaffected member agree to partici-pate in the study by providing a sample, or whose DNA is already available and extracted using a method known and validated by the steering committee.\n\n    * For all related members of undiagnosed families who have agreed to participate:\n  * Have at least two other family members who have agreed to participate in the study.\n  * Agree to provide a blood sample or have DNA already available in sufficient quantity and extracted using a method known and validated by the steering committee.\n  * Patient willing to undergo a skin biopsy if not previously obtained.\n  * Be affected by a neurological disease candidate for these repeats, for which genomic data did not reveal mutations or expansions in known genes, or be unaffected and have had a neurological examination showing no signs related to any of the neurological diseases candidate for these repeats.\n* For controls :\n\nParticipant for whom:\n\n* a consultation is scheduled at CHU Bordeaux for a reason other than a neurological disorder, has agreed to a neurological examination showing no signs of neurological disease, and has agreed to a blood draw and skin biopsy, or\n* the samples required for the study are already available in sufficient quantity in the CHU Bordeaux biobank and extracted using a method known and validated by the steering committee, or\n* accompanying a patient attending a consultation at CHU Bordeaux, showing no signs of neurologi-cal disease, and agreeing to a blood draw and skin biopsy, or whose samples are already available in sufficient quantity and extracted using a method known and validated by the steering committee.\n\nExclusion Criteria:\n\nFor all participants:\n\n• Refusal to participate in research: Refusal to provide informed consent or opposition to the use of these samples.\n\n* By the parents or the holder of parental authority for patients under the age of 18\n* By the patient's representative for adults under guardianship\n* By the adult patient This opposition from the patient must be communicated to the site investigator within a maximum of one month after the information note has been sent. If the letter confirming consent is returned due to an incorrect address, the patient will not be included.\n\n  * Degraded DNA or average size \\\u003C 30 kb",true,"ALL","6 Years","60 Years",{"count":22,"type":23},304,"ESTIMATED","INTERVENTIONAL",[26],"NA","Nucleotide repeats emerge as one of the most prolific classes of genetic variations. They have the propensity to in-crease in length across generations, and have been implicated in at least 65 known neurological\u002F neurodevelop-mental and neuromuscular conditions. Simultaneous analysis of all these nucleotide repeats is now possible through the cutting-edge methodologies recently developed that are the long-read sequencing and the optical genome mapping. Investigator propose to test these methodologies in patients carrying expansions in those repeats and to determine the capacity of these technics to detect novel repeats in patients with no genetic diagnosis yet.",[29],"Neurogenetic Diseases",[31,32,33,34,35],"long read sequencing","genetic diagnosis","cytogenetics","nucletotide repeat expansion","neurogenetic disease","NOT_YET_RECRUITING","2026-06-18",{"date":39,"type":40},"2026-06-24","ACTUAL",{"date":42,"type":23},"2026-09",{"date":44,"type":23},"2028-09",{"name":46,"class":47},"University Hospital, Bordeaux","OTHER",{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":52,"acronym":53,"eligibilityCriteria":54,"healthyVolunteers":17,"sex":18,"minAge":4,"maxAge":4,"enrollmentInfo":55,"targetDuration":4,"studyType":24,"phases":57,"briefSummary":58,"conditions":59,"keywords":60,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":67,"completionDateStruct":69,"leadSponsor":71,"locationsCount":73},"100589531","use-of-omics-methods-to-classify-variations-of-uncertain-significance-and-improve-diagnosis-of-neurogenetic-diseases-100589531","NCT06955624","Use of Omics Methods to Classify Variations of Uncertain Significance and Improve Diagnosis of Neurogenetic Diseases","OMID-NEURO","Inclusion Criteria:\n\nFor this project, the inclusion of 3 participant profiles is required:\n\n* 1a. Patient, major or minor, with a neurological disease affecting the central nervous system, who has already benefited from a genomic analysis (panel, exome or genome sequencing) as part of routine care, with inconclusive analysis because the result was either a variation of uncertain significance or the absence of a variant of interest (patients with inconclusive genomic results).\n* 1b. Patient with neurological disease affecting the central nervous system, of confirmed monogenic or probable oligogenic cause (positive controls).\n* A relative of a type 1a. or 1b. patient with no symptoms of the disease, after the expected age of onset of symptoms in the patient's own family (healthy relatives).\n\nFor all 3 groups:\n\n* Affiliation with a social security scheme\n* Agreement to take part in the study with signature of a specific informed consent form for the study.\n\nExclusion Criteria:\n\nFor patients with inconclusive results: Patient with a neurological disease not suspected of a monogenic or oligogenic cause\n\nFor healthy relatives: existence of a neurological disease (other than uncomplicated migraine) or psychiatric disease (other than simple anxiety stable under treatment).\n\n\\-",{"count":56,"type":23},95,[26],"Many neurological disorders show a strong genetic basis, from hereditary diseases caused by a single mutation in a given gene, to diseases caused by combinations of strong genetic risk factors. However, even after the sequencing of the appropriate genes, a large proportion of patients remains undiagnosed, either because there is no candidate mutation observed, or in case of identification of a candidate mutation with insufficient knowledge to consider it as pathogenic or not.\n\nThe aim of this project is to identify the cause of neurogenetic diseases in patients in situations of diagnostic wandering or dead ends by proposing the analysis of RNA and\u002For proteins from different tissues.",[29],[61,62],"Neurogenetic diseases","Central nervous system disease","RECRUITING","2025-04-24",{"date":66,"type":40},"2025-05-02",{"date":68,"type":40},"2025-01-15",{"date":70,"type":23},"2031-01-15",{"name":72,"class":47},"University Hospital, Rouen",1]