La relation entre l’autisme et les syndromes d’Ehlers-Danlos/troubles du spectre de l’hypermobilité

Titre original en anglais : The Relationship between Autism and Ehlers-Danlos Syndromes/Hypermobility Spectrum Disorders

Cette publication est incluse dans le projet « Contributions académiques de personnes autistes sur l’autisme ». un auteur·ice de cette publication est identifié·e comme autiste dans le projet.

À propos de la mention auteur·ice autiste

Casanova, M., Baeza-Velasco, C., Buchanan, C. B., & Casanova, M. F. (2020). The Relationship between Autism and Ehlers-Danlos Syndromes/Hypermobility Spectrum Disorders. Journal of Personalized Medicine, 10(4), 260. https://doi.org/10.3390/jpm10040260

Publication date: 01/12/2020 Ajout dans AutiHub: 14/09/2026 Type: Article Langue de l’article: Anglais

Cette publication est intégrée dans AutiHub via :

Auteurs

Auteur·ices des publications
4
Auteur·ices de la publication identifié·es comme autistes
1 / 4 (25,0 %)

Résumé

Un intérêt considérable est apparu concernant la relation entre les troubles héréditaires du tissu conjonctif tels que les syndromes d’Ehlers-Danlos (EDS)/troubles du spectre de l’hypermobilité (HSD) et l’autisme, tant en termes de comorbidité que de cooccurrence au sein des mêmes familles. Cet article passe en revue l’état actuel de nos connaissances, tout en mettant en évidence les questions non résolues concernant ce remarquable groupe de patients, qui, nous l’espérons, suscitera un intérêt scientifique accru dans les années à venir. En particulier, les patients eux-mêmes demandent davantage de recherches dans ce domaine d’intérêt croissant, bien que la science ait été lente à répondre à cet appel. Nous examinons ici le chevauchement entre ces deux affections de spectre, y compris les similitudes neurocomportementales, psychiatriques et neurologiques, les neuropathies périphériques et neuropathologies communes, ainsi qu’une dysrégulation autonome et immunitaire similaire. Ensemble, ces données mettent en évidence la parenté potentielle entre ces deux affections et suggèrent que les EDS/HSD pourraient représenter un sous-type d’autisme.

Considerable interest has arisen concerning the relationship between hereditary connective tissue disorders such as the Ehlers-Danlos syndromes (EDS)/hypermobility spectrum disorders (HSD) and autism, both in terms of their comorbidity as well as co-occurrence within the same families. This paper reviews our current state of knowledge, as well as highlighting unanswered questions concerning this remarkable patient group, which we hope will attract further scientific interest in coming years. In particular, patients themselves are demanding more research into this growing area of interest, although science has been slow to answer that call. Here, we address the overlap between these two spectrum conditions, including neurobehavioral, psychiatric, and neurological commonalities, shared peripheral neuropathies and neuropathologies, and similar autonomic and immune dysregulation. Together, these data highlight the potential relatedness of these two conditions and suggest that EDS/HSD may represent a subtype of autism.

Bibliographie citée par cette référence

Les références citées sont importées depuis des sources externes de métadonnées lorsqu’elles sont disponibles. La liste peut être partielle.

Vue d’ensemble de la bibliographie citée

Ces indicateurs décrivent la bibliographie citée par cette publication. Un nom d’auteurice est compté chaque fois qu’il apparaît dans une référence citée : une même personne peut donc être comptée plusieurs fois. Les noms qui ne sont pas encore associés à un·e auteurice déjà présent·e dans AutiHub sont traités comme inconnus, pas comme non autistes. Dernier calcul : 14/09/2026 14:22.

Références citées
148
Avec un DOI
138
Sans DOI, à partir du texte brut de la bibliographie
9
6 / 148 (4,1 %) références citées comprennent au moins une personne identifiée comme autiste.
Références avec données à compléter
5 / 148 (3,4 %)
Références avec noms d’auteurices détectés
143 / 148 (96,6 %)
Sans nom d’auteurice détecté
5
Sans titre structuré
4
Sans identifiant stable
7
Références avec noms bruts d’auteurices restant à vérifier
4
Références avec problème de récupération des métadonnées externes
1
Ces indicateurs portent sur les références citées affichées sur cette page, après fusion des doublons techniques. Une référence sans DOI peut quand même soutenir les statistiques d’auteurices lorsqu’un titre et des noms d’auteurices sont disponibles.
Noms d’auteurices détectés dans la bibliographie citée
940
À partir du DOI ou de métadonnées externes
940
À partir du texte brut validé de la bibliographie
0
Noms bruts déjà validés
0
Noms bruts restant à vérifier
4
112 / 940 (11,9 %) noms sont associés à un·e auteurice déjà présent·e dans AutiHub. 828 / 940 (88,1 %) noms ne sont pas encore associés.
Noms associés à une personne identifiée comme autiste
7 / 940 (0,7 %)
Calculé sur l’ensemble des noms d’auteurices détectés dans la bibliographie citée. Parmi les noms associés à un·e auteurice déjà présent·e dans AutiHub : 7 / 112 (6,2 %). Personnes distinctes identifiées comme autistes : 3 / 825 (0,4 %).
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