דילוג לניווט ראשי דילוג לחיפוש דילוג לתוכן הראשי

Prevalence and Association of Generalized Joint Hypermobility in Children with Functional Neurological Disorder: A Retrospective Study

  • Jana Landa
  • , Karin Mashevich
  • , Etzyona Eisenstein
  • , Sharon Barak

פרסום מחקרי: פרסום בכתב עתמאמרביקורת עמיתים

תקציר

Aims: Functional neurological disorder (FND) etiology is multifactorial. This study aimed to examine: (1) generalized joint hypermobility (GJH) prevalence in children diagnosed with FND and (2) the association between GJH and FND severity, activity level, and participation. Methods: Participated in this study 53 children with FND (mean age 14.2 ± 2.7 years; 73.6% female). GJH was assessed using the Beighton score. FND severity was evaluated with the 24-item Children’s Somatic Symptoms Inventory (CSSI-24), number of limbs affected, and pain following the six-minute walk test (6MWT). Results: GJH was identified in 43% (Beighton ≥4) and 24% (Beighton ≥6) of participants. Elbow hyperextension was the most common feature (56.6%). The total Beighton score was independently associated with CSSI-24 (R2=.25, p<.01) and with the number of limbs involved (R2=.15, p<.01). A positive association was observed between Beighton score and pain post-6MWT. Conclusion: Regardless of the Beighton cutoff used, GJH prevalence remained high, with at least 1 in 4 participants presenting GJH even at the strictest threshold (≥6). GJH was associated with increased CSSI-24 and motor involvement. These findings suggest that GJH may represent a somatic vulnerability factor within the biopsychosocial model of FND. Routine assessment could help identify meaningful subgroups and guide individualized treatment.

שפה מקוריתאנגלית
כתב עתPhysical and Occupational Therapy in Pediatrics
מזהי עצם דיגיטלי (DOIs)
סטטוס פרסוםהתקבל/בדפוס - 2026

טביעת אצבע

להלן מוצגים תחומי המחקר של הפרסום 'Prevalence and Association of Generalized Joint Hypermobility in Children with Functional Neurological Disorder: A Retrospective Study'. יחד הם יוצרים טביעת אצבע ייחודית.

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