Evidence map›Paper›PMID 42482093›Full record

ArticleOrphanet journal of rare diseases2026

Eating behaviour phenotype in the MYT1L-related neurodevelopmental disorder: a deep phenotyping study using standardized questionnaires.

Juliette Coursimault, Emilie Guillon, François Lecoquierre, Camille Charbonnier, Anne-Marie Guerrot, Alice Goldenberg, Gaël Nicolas, Elise Schaefer, Anael Ayrolles, Richard Delorme and 17 more

Abstract readMulticenter Study
In one paragraph

Article in Orphanet journal of rare diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

27 authors.

Juliette CoursimaultDepartment of Genetics and Reference Center for Developmental Disorders, Univ Rouen Normandie, Normandie Univ, Inserm U1245 and CHU Rouen, Rouen, F-76000, France. j.coursimault@chu-rouen.fr.
Emilie GuillonNutrition Department, Reference Center for Rare Diseases PRADORT, Assistance Publique Hôpitaux de Paris, Pitié-Salpêtrière Hospital, Paris, France.
François LecoquierreDepartment of Genetics and Reference Center for Developmental Disorders, Univ Rouen Normandie, Normandie Univ, Inserm U1245 and CHU Rouen, Rouen, F-76000, France.
Camille CharbonnierDepartment of Genetics and Reference Center for Developmental Disorders, Univ Rouen Normandie, Normandie Univ, Inserm U1245 and CHU Rouen, Rouen, F-76000, France.
Anne-Marie GuerrotDepartment of Genetics and Reference Center for Developmental Disorders, Univ Rouen Normandie, Normandie Univ, Inserm U1245 and CHU Rouen, Rouen, F-76000, France.
Alice GoldenbergDepartment of Genetics and Reference Center for Developmental Disorders, Univ Rouen Normandie, Normandie Univ, Inserm U1245 and CHU Rouen, Rouen, F-76000, France.
Gaël NicolasDepartment of Genetics and Reference Center for Developmental Disorders, Univ Rouen Normandie, Normandie Univ, Inserm U1245 and CHU Rouen, Rouen, F-76000, France.
Elise SchaeferService de Génétique Médicale, Institut de Génétique Médicale d'Alsace (IGMA), Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
Anael AyrollesDepartment of Child and Adolescent Psychiatry, APHP.Nord, Robert Debré University Hospital, Paris Cité University, Paris, France.
Richard DelormeDepartment of Child and Adolescent Psychiatry, APHP.Nord, Robert Debré University Hospital, Paris Cité University, Paris, France.
Florence RiccardiGénétique Médicale, Centre Hospitalier Intercommunal Toulon - La Seyne- sur-Mer, Toulon, France.
Maude GreletGénétique Médicale, Centre Hospitalier Intercommunal Toulon - La Seyne- sur-Mer, Toulon, France.
Roseline CaumesUniversité de Lille, CHU de Lille, Clinique de Génétique «Guy Fontaine», EA7364 RADEMEF-59000, Lille, France.
Mathilde NizonService de Génétique Médicale, CHU Nantes, Nantes, France.
Bertrand IsidorService de Génétique Médicale, CHU Nantes, Nantes, France.
Guillaume JouretNational Center of Genetics (NCG), Laboratoire National de Santé (LNS), Dudelange, L- 3555, Luxembourg.
Caroline RooryckUniv. Bordeaux, MRGM INSERM U1211, CHU de Bordeaux, Service de Génétique Médicale, Bordeaux, F-33000, France.
Jeanne AmielService de Médecine Génomique des Maladies Rares, Hôpital Necker- Enfants Malades, AP-HP, Paris, France.
Anne-Sophie AlaixService de Médecine Génomique des Maladies Rares, Hôpital Necker- Enfants Malades, AP-HP, Paris, France.
Victor MorelDepartment of Medical Genetics, La Timone Hospital, AP-HM, La Timone Children's Hospital, Marseille, France.
Adeline JacquinetDepartment of Genetics, Sart Tilman University Hospital, Liège, Belgium.
Cyril MignotDépartement de Génétique, Groupe Hospitalier Pitié-Salpêtrière-Hôpital Trousseau Centre de Référence Déficiences Intellectuelles de Causes Rares, APHP.Sorbonne Université, Paris, France.
Laurence FaivreUniversité Bourgogne Europe, CHU Dijon Bourgogne, Inserm, CTM UMR1231, équipe GAD, FHU TRANSLAD, Centre de génétique, Centre de référence Anomalies du Développement et Syndromes Malformatifs, Centre de référence Déficiences Intellectuelles de Causes Rares, et Centre de référence GénoPsy, Dijon, 21000, France.
Emilie Fraile-CaiettaService de pédiatrie, Centre Hospitalier de Toulon, Toulon, France.
Sarah ChalopinNutrition Department, Reference Center for Rare Diseases PRADORT, Assistance Publique Hôpitaux de Paris, Pitié-Salpêtrière Hospital, Paris, France.
Béatrice DubernSorbonne Université, Inserm, Nutrition and Obesities: Systemic Approaches, NutriOmique Research Group, Paris, France.
Christine PoitouNutrition Department, Reference Center for Rare Diseases PRADORT, Assistance Publique Hôpitaux de Paris, Pitié-Salpêtrière Hospital, Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe MYT1L-related neurodevelopmental disorder (MRND) is associated with global motor and language delay, intellectual disability, behavioural disturbances, epilepsy and frequent early-onset obesity. Eating disturbances have been reported but remain poorly characterized. A systematic characterization of the eating behaviour phenotype is essential to improve diagnosis and management.

methodsWe conducted a multicentre study including 21 French-speaking individuals with a molecularly confirmed MRND and either overweight/obesity or eating behaviour disturbances. Eating behaviours were reported by relatives using validated questionnaires widely employed in rare obesity research: the Dykens Hyperphagia Questionnaire (HQ), the Trousseau Impulsivity Questionnaire, the Children's Eating Behaviour Questionnaire (CEBQ), the Food Cravings Questionnaire-Trait-reduced (FCQ-T-r, adults only), and a Visual Analogue Scale (VAS) for hunger. When available, questionnaire results were compared with published studies using the same instruments.

resultsPersistent hyperphagic behaviours were identified in the majority of patients, with the HQ questionnaire highlighting sustained food-seeking behaviours and pervasive food preoccupation. The mean global score was 25.9, indicating a moderate yet sustained hyperphagic profile. CEBQ revealed a strong attraction to food combined with reduced satiety responsiveness and rapid eating. Hunger was reported as persistent throughout the day. In children food impulsivity was less frequent (5/14; 36%) and no correlation was found between impulsivity and hyperphagia severity, contrasting with findings in other obesity syndromes. Among adults, 62.5% had scores suggestive of food addiction (FCQ-T-r ≥ 50).

conclusionThis study delineates an eating behaviour profile in a symptom-enriched subgroup of individuals with MRND, characterized by moderate but sustained hyperphagia, persistent hunger, impaired satiety, low food-related impulsivity in children but frequent food craving/addiction in adults. These findings support early, age-adapted and multidisciplinary management strategies and highlight the need for targeted interventions to reduce the burden on affected individuals and families.

Indexed as

Feeding BehaviorNeurodevelopmental DisordersAdolescentAdultChildChild, PreschoolFeeding and Eating DisordersFemaleHumansHyperphagiaMaleObesityPhenotypeSurveys and QuestionnairesYoung Adult2p25.3 deletionDeep phenotypic characterizationDykensEating behavioursMYT1L haploinsufficiencyRare diseaseStandardized questionnairesSyndromic obesity

Identifiers

PMID42482093
PMCPMC13685170

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.