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Recruiting NCT07008612

MYT1L Syndrome: a Rare Paediatric Genetic Syndrome Responsible for a Neurodevelopmental Disorder

No phase Interventional MYT1L Syndrome

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Patients with a genetic syndrome linked to the MYT1L gene, Patients with a neurodevelopmental disorder of genetic origin but not linked to MYT1L.
Who it may be relevant to
Registry conditions: MYT1L Syndrome. Basic parameters: from 6 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Characterisation of Language and Prosody Disorders, Cognitive Functioning and Behavioural Problems in MYT1L Syndrome

Overview

MYT1L syndrome is a rare genetic syndrome, recently described in 2011, with paediatric onset, responsible for a neurodevelopmental disorder combining psychomotor retardation, learning difficulties and/or intellectual development disorders, epilepsy, overweight and eating disorders. The Rouen genetics department is currently positioned as a clinical expert in this disease. The study published in 2020 by our team (Coursimault J et al., Hum Genet. 2022, PMID: 34748075) has enabled us to describe 40 new individuals worldwide, to gain a better understanding of this disease, to specify the genotype-phenotype relationships and to describe new clinical signs. We were able to confirm the presence of a neurodevelopmental disorder in 100% of patients, which includes: language delay, impaired orality, global and facial hypotonia, prosodic features and behavioural problems. This will be the first study in the world to characterise the neuropsychological, language and prosodic profiles of MYT1L patients.

Detailed description

Although neuropsychological and speech therapy assessment is part of the routine work-up of any patient with a neurodevelopmental disorder, the heterogeneous use of assessment scales has not made it possible to obtain a precise characterisation of the neuropsychological and language profile of patients with MYT1L syndrome in retrospective studies. As a result, it is not possible to establish specific language and behavioural rehabilitation treatments. The aim of the study is to provide substantiated information on language (oral language, speech), prosody (reception and expression) and cognitive-behavioural aspects (global IQ, executive functions, sensory profile, attention, aggression, intolerance to frustration, anxiety). This project proposes to carry out a protocol used in routine care to assess language, prosody, cognitive functions and mood disorders, with the aim of identifying a specific language, prosody, cognitive and behavioural profile of patients with MYT1L syndrome, which could lead to better assessment in the future, screening for disorders and better targeting of rehabilitation in future patients, and to identify profiles suggestive of MYT1L syndrome in patients who have not had genetic confirmation (no variation identified or variation of uncertain significance).

Interventions

  • Diagnostic test Patients with a genetic syndrome linked to the MYT1L gene
    * Neuropsychological assessment by the neuropsychologist (lasting 1h30) * Speech and language assessment (including language and prosody) by the speech therapist, lasting 1h30
  • Diagnostic test Patients with a neurodevelopmental disorder of genetic origin but not linked to MYT1L
    Evaluation de la prosodie par l'orthophoniste (45 minutes)

Primary outcome measures

  • Speech-language profile [Time frame: At enrollment visit]
Secondary outcome measures (3)
  • Speech-language profile [Time frame: At enrollment visit]
  • Prosodic speech therapy profile (patients with MYT1L syndrome) [Time frame: At enrollment visit]
  • Prosodic speech therapy profile (patients with a molecular diagnosis other than MYT1L) [Time frame: At enrollment visit]

Eligibility criteria

Inclusion criteria

MYT1L Group Patients

  • Minimum age for inclusion: 6 years
  • Maximum age for inclusion: no upper age limit
  • Language: French
  • Consent of parents or legal guardian
  • Social security coverage required

Prosody Group Patients

  • Unaided visual or hearing impairment making assessments impossible
  • Non-French speaking patients
  • Patients with a dual molecular genetic diagnosis also causing a neurodevelopmental disorder
  • Acquired neurological disorder

Exclusion criteria

MYT1L Group patients

  • Unaided visual or hearing impairment making assessments impossible
  • Non-French speaking patients
  • Patients with a dual molecular genetic diagnosis also causing a neurodevelopmental disorder
  • Acquired neurological disorder

Prosody Group Patients

  • Patients with molecularly confirmed MYT1L syndrome.
  • Nonverbal patients

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Non-randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Treatment

Study locations

France · 1 center
  • University Hospital of Rouen — Rouen

Identifiers

NCT: NCT07008612 · 2024/0255/HP · 2024-A02492-45

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗