Short-term amelioration of dysarthria after Zolpidem intake in a patient with primary familial brain calcification: a case report
Publication date
2026-01-15
Editors
Advisors
Supervisors
Document Type
Article
Metadata
Show full item recordCollections
License
cc_by
Abstract
Purpose: Transient improvement of aphasia, motor impairment, and disorders of consciousness after the use of zolpidem, a sedative, has been reported in several movement disorders and hyporesponsive syndromes. Here, we present a patient with Primary Familial Brain Calcification (PFBC), a rare neurodegenerative disease characterized by basal ganglia calcification, who experienced a transient improvement in speech following zolpidem administration. Methods: Serendipitously, a 40-year-old female with PFBC and severe dysarthria experienced transient amelioration of dysarthria after treatment with zolpidem, which was prescribed for insomnia. We carried out a comprehensive clinical assessment before and three hours after administration of zolpidem tartrate 10 mg, including standardized evaluations of speech, aphasia, motor function, and patient-perceived difficulties. Results: A transient improvement in speech was confirmed after zolpidem intake. However, notable side effects occurred, including worsening of fine motor control, coordination, postural stability, and bradykinesia. Conclusions: This case suggests that zolpidem can influence PFBC related neurological symptoms, identifying the facilitation of internal globus pallidus inhibition as a new therapeutic target. Its use in individual patients warrants the weighing of positive and negative clinical effects, patients’ personal preferences, and wearing-off which invariable occurs after repeated use.
Keywords
Case report, Dysarthria, MYORG, Primary familial brain calcification, Zolpidem, Genetics(clinical), Pharmacology (medical)
Citation
Snijders, B M G, van Erp, W S, Storm, M, Netjes, J A, van Valen, E, Bakker, S, Peters, M J L, de Jong, P A, Emmelot-Vonk, M H & Koek, H L 2026, 'Short-term amelioration of dysarthria after Zolpidem intake in a patient with primary familial brain calcification : a case report', Journal of Rare Diseases (Germany), vol. 5, no. 1, 3. https://doi.org/10.1007/s44162-025-00142-6