# Clinical features of adolescent-onset functional motor disorders in tertiary movement disorders centers

**Authors:** Christian Geroin, Tommaso Ercoli, Enrico Marcuzzo, Angela Sandri, Serena Camozzi, Domenico Maddaloni, Luigi Michele Romito, Roberto Eleopra, Lucia Tesolin, Serena Pellegrin, Alessandra Nicoletti, Giovanni Mostile, Alessandro Magliozzi, Andrea Pilotto, Nicola Modugno, Enrica Olivola, Benedetta Demartini, Veronica Nisticò, Roberto Erro, Sofia Cuoco, Alessandro Tessitore, Rosa De Micco, Roberto Ceravolo, Eleonora Del Prete, Carlo Dallocchio, Carla Arbasino, Marcello Esposito, Trinchillo Assunta, Francesco Bono, Angelo Pascarella, Martina Petracca, Paola Zinzi, Giovanni Fabbrini, Gina Ferrazzano, Laura Bonanni, Sara Varanese, Alberto Albanese, Paola Polverino, Valentina Baglioni, Giovanni Defazio, Maurizio Zibetti, Paolo Manganotti, Paolo Solla, Giovanna Calandra-Buonaura, Antonio Pisani, Michele Tinazzi

PMC · DOI: 10.1007/s00415-026-13761-w · Journal of Neurology · 2026-03-22

## TL;DR

This study examines the clinical features of adolescent-onset functional motor disorders, finding they are common and linked to specific non-motor symptoms and diagnostic delays.

## Contribution

The study identifies distinct clinical and demographic features of adolescent-onset functional motor disorders compared to adult-onset cases.

## Key findings

- Adolescent-onset FMDs are associated with longer disease duration and more medical consultations before diagnosis.
- Functional seizures and infections are more common in adolescent-onset FMDs compared to adult-onset cases.
- Adolescent-onset FMDs show lower rates of insomnia, fatigue, and antipsychotic use.

## Abstract

Functional Motor Disorders (FMDs) represent a diagnostic and therapeutic challenge in pediatric neurology, particularly among adolescents. Their clinical presentation is common but often nonspecific, leading to frequent misdiagnoses and diagnostic delays. We aimed to characterize FMDs in adolescents and to examine the frequency of isolated and combined phenotypes and their associations with demographic and clinical variables.

In this observational study, data were obtained from the Italian Registry of FMDs, including patients with a clinically definite diagnosis of FMD consecutively enrolled at 25 Italian tertiary movement disorders centers.

Among 847 patients, 93 (10.9%) had adolescent-onset FMDs. Motor phenotypes did not differ significantly between adolescent- and adult-onset FMDs, with the exception of parkinsonism, which was observed only in the latter. Compared with adult-onset FMDs, adolescent-onset FMDs were associated with a longer disease duration, a higher number of medical consultations before diagnosis, and a higher frequency of functional seizures and infections, but with lower rates of insomnia, fatigue, and antipsychotic use. In multivariable analysis, adolescent-onset FMDs remained independently associated with a greater number of medical consultations (adjusted OR 1.07; 95% CI 1.02–1.13), the presence of functional seizures (adjusted OR 2.06; 95% CI 1.09–3.8), and with lower occurrence of insomnia (adjusted OR 0.49; 95% CI 0.27–0.92) and fatigue (adjusted OR 0.51; 95% CI 0.30–0.86). Pain was more likely to be associated with the combined FMDs phenotype.

Adolescent-onset FMDs are common and are associated with several non-motor symptoms in tertiary movement disorders centers. Early and accurate diagnosis may help to reduce unnecessary investigations and inappropriate treatments.

The online version contains supplementary material available at 10.1007/s00415-026-13761-w.

## Linked entities

- **Diseases:** insomnia (MONDO:0013600)

## Full-text entities

- **Diseases:** trauma (MESH:D014947), infections (MESH:D007239), sensory disturbances (MESH:D012678), panic attacks (MESH:D016584), depression (MESH:D003866), paroxysmal kinesigenic dyskinesia (MESH:C537180), dystonia (MESH:D004421), Epileptic Seizures (MESH:D004827), abnormal movements (MESH:D004409), autism (MESH:D001321), long-term (MESH:D000088562), cognitive or physical impairment (MESH:D003072), Parkinson's Disease (MESH:D010300), sleep disorders (MESH:D012893), Psychiatric comorbidities (MESH:D001523), obsessive-compulsive disorder (MESH:D009771), Functional weakness (MESH:D018908), Pain (MESH:D010146), facial disorders (MESH:D005155), episodic ataxia (MESH:C580065), neurological conditions (MESH:D019636), rigidity (MESH:D009127), headache (MESH:D006261), auditory dysfunction (MESH:D006311), neurological disease (MESH:D020271), neurodevelopmental conditions (MESH:D020763), Tourette syndrome (MESH:D005879), truncal weakness (MESH:D001259), vision (MESH:D014786), gait disorders (MESH:D020233), FMDs (MESH:D003291), migraine (MESH:D008881), psychogenic movement disorder (MESH:D018781), Parkinsonism (MESH:D010302), Movement Disorders (MESH:D009069), jerks (MESH:D009207), insomnia (MESH:D007319), dopa (MESH:C538007), Wilson disease (MESH:D006527), fatigue (MESH:D005221), neurological (MESH:D009461), FMD (MESH:C536391), tremor (MESH:D014202), bradykinesia (MESH:D018476), seizure (MESH:D012640), inflammatory disorders (MESH:D007249), motor disorders (MESH:D000068079), tic-like behaviors (MESH:D020323), anxiety (MESH:D001007)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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Source: https://tomesphere.com/paper/PMC13006462