# Case Report: Intensive multidisciplinary motor-cognitive rehabilitation treatment in Gerstmann–Sträussler–Scheinker syndrome

**Authors:** A. De Laurenzis, C. Siri, L. Bandirali, L. Lucca, L. Covaia, F. Ferrari, C. Zaffina, M. Canesi

PMC · DOI: 10.3389/fresc.2025.1599247 · Frontiers in Rehabilitation Sciences · 2026-01-23

## TL;DR

A 34-year-old woman with Gerstmann–Sträussler–Scheinker syndrome showed improved autonomy after intensive motor-cognitive rehabilitation.

## Contribution

This case report demonstrates the effectiveness of tailored motor-cognitive rehabilitation in managing GSS symptoms.

## Key findings

- After 4 weeks of rehabilitation, the patient showed improved balance and autonomy (Barthel Index increased from 60 to 70).
- The intervention led to gains in basic and instrumental activities of daily living.
- The case emphasizes the role of multidisciplinary rehabilitation in enhancing quality of life for GSS patients.

## Abstract

Gerstmann–Sträussler–Scheinker syndrome (GSS) is a genetic, autosomal dominant prion brain disease that causes ataxia and slow cognitive decline. Herein, we describe a 34-year-old woman (S.C.B.) diagnosed with GSS (variant Pro102Leu). In 2018, she presented with gait instability without falls, early fatigue, and dizziness; after 3 years, urinary incontinence, initial insomnia and rapid-eye movement sleep behavior disorder, writing difficulties, and occasional dysphagia had appeared. S.C.B. was admitted to the Neurorehabilitation Unit due to the progressive worsening of her balance and walking ability [Timed Up and Go (TUG): not evaluated; Berg Balance Scale (BERG): 5/56]. At admission, neurological, neuropsychological, physiotherapeutic, occupational, and speech assessments were performed. She was completely dependent in basic (ADL) and instrumental activities of daily living (iADL) (ADL: 5/6; iADL: 4/8; Barthel Index: 60); furthermore, moderate cognitive decline and depressive symptoms were observed. After 4 weeks of intensive motor-cognitive rehabilitation treatment, an improvement was observed in all the intervention areas, leading to a global gain in autonomy (TUG: 1 min 50 s; BERG: 10/56; Barthel Index: 70). This case report highlights the importance of tailored motor-cognitive rehabilitation and how these interventions can enhance patients’ quality of life and their ability to cope with their symptoms. In conclusion, this case contributes to a broader understanding of treatment options that clinicians can propose to patients.

## Full-text entities

- **Diseases:** cognitive decline (MESH:D003072), falls (MESH:C537863), ataxia (MESH:D001259), prion brain disease (MESH:D017096), depressive symptoms (MESH:D003866), dizziness (MESH:D004244), insomnia (MESH:D007319), GSS (MESH:D016098), urinary incontinence (MESH:D014549), writing difficulties (MESH:D020195), rapid-eye movement sleep behavior disorder (MESH:D020187), gait instability (MESH:D043171), fatigue (MESH:D005221), dysphagia (MESH:D003680)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** Pro102Leu

## Full text

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## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC12876179/full.md

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Source: https://tomesphere.com/paper/PMC12876179