Version 1
: Received: 22 February 2024 / Approved: 26 February 2024 / Online: 26 February 2024 (11:45:00 CET)
How to cite:
R. Santos, E. A Comprehensive Review of Secondary Movement Disorders. Preprints2024, 2024021435. https://doi.org/10.20944/preprints202402.1435.v1
R. Santos, E. A Comprehensive Review of Secondary Movement Disorders. Preprints 2024, 2024021435. https://doi.org/10.20944/preprints202402.1435.v1
R. Santos, E. A Comprehensive Review of Secondary Movement Disorders. Preprints2024, 2024021435. https://doi.org/10.20944/preprints202402.1435.v1
APA Style
R. Santos, E. (2024). A Comprehensive Review of Secondary Movement Disorders. Preprints. https://doi.org/10.20944/preprints202402.1435.v1
Chicago/Turabian Style
R. Santos, E. 2024 "A Comprehensive Review of Secondary Movement Disorders" Preprints. https://doi.org/10.20944/preprints202402.1435.v1
Abstract
Secondary movement disorders (SMDs) represent a heterogeneous group of neurological conditions characterized by abnormal, involuntary movements resulting from various underlying causes. This comprehensive review aims to thoroughly understand SMDs, including their epidemiology, pathophysiology, clinical manifestations, diagnostic approach, and management strategies. SMDs encompass a spectrum of movement abnormalities, including dystonia, chorea, athetosis, myoclonus, tics, and tremors. They can arise from a multitude of etiologies, such as drug-induced effects, post-infectious processes, metabolic disturbances, and structural brain lesions. The epidemiology of SMDs varies depending on the underlying cause, with some conditions being more prevalent in specific populations or age groups. Understanding the pathophysiology of SMDs is crucial for accurate diagnosis and targeted management. Diagnosing SMDs requires a comprehensive approach, including a detailed history, physical examination, laboratory investigations, neuroimaging studies, and sometimes electrophysiological studies. Management of SMDs is multifaceted and may involve pharmacological, non-pharmacological, and surgical interventions. Individualized treatment plans are essential, considering the underlying cause, severity of symptoms, and patient preferences. Emerging concepts in the field of SMDs include advancements in genetic research, identification of biomarkers, and development of novel therapeutic approaches. There is a growing focus on patient-centered care and improving the quality of life for individuals with SMDs. In conclusion, SMDs pose diagnostic and therapeutic challenges, requiring a multidisciplinary approach for optimal management. Continued research and collaboration are essential for advancing our understanding and treatment of these complex disorders.
Keywords
secondary movement disorders; dystonia; chorea; athetosis; myoclonus; tics; tremor; drug-induced movement disorders; post-infectious movement disorders; metabolic disorders
Subject
Medicine and Pharmacology, Internal Medicine
Copyright:
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.