Split limb phenomenon in amyotrophic lateral sclerosis: electrophysiologic study
نویسندگان
چکیده
Abstract Background Amyotrophic lateral sclerosis (ALS) is a degenerative disease that affects the upper and lower motor neurons. The onset of frequently focal, usually involving distal segments extremities. A dissociated pattern muscle atrophy commonly found in hands feet. This study aims to investigate presence (if any) split indices ALS patients correlate these with confounding factors. total 48 people were studied. control group consists 24 another age- gender-matched patients. To assess functional status strength, rating scale (ALSFRS) Medical Research Council (MRC) used, respectively. Sensory nerve conduction, as well compound action potential (CMAP) amplitude, recorded from muscles limbs. electromyographic (EMG) activity 20 unit potentials (MUAPs) four different areas was also Results Distal CMAP amplitude reduced all tested (especially noticed when comparing reciprocal muscles). In patients, foot index (SFI) significantly higher, while elbow (SEI) lower. be negatively related duration, but positively ALSFRS scores. MRC score. Conclusion Ankle dorsiflexion are more involved (dissociated) than plantar flexor muscles, flexors extensors. SFI correlates duration
منابع مشابه
Amyotrophic lateral sclerosis presenting as typical split hand syndrome.
To cite: Nalabothu M, Monigari N, Vellalacheruvu N, et al. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2014207647 DESCRIPTION A 38-year-old man presented to a hospital with weakness of both hands (right>left) with associated generalised weakness for the past 2 years. The patient initially noticed weakness and thinning of his right hand followed by the left for...
متن کاملAmyotrophic Lateral Sclerosis in a Patient with Behçet’s Disease
Behçet’s disease is a multisystem vasculitis. Its neurological involvement mostly includes parenchymal and non-parenchymal central nervous system manifestations. Peripheral nervous system presentations are rare. A 32-yr-old male patient who fulfilled the international study group criteria for Behçet’s disease, referred to our center with walking difficulty and repeated falling downs. Neurologi...
متن کاملAmyotrophic Lateral Sclerosis
Touch MEdical MEdia 53 Fasciculation, which is observed in various peripheral motor neuron disorders, is most frequently found in nonprogressive benign fasciculation syndrome (BFS). Patients with BFS never exhibit muscle atrophy or pathologic weakness and not all such patients visit hospitals; therefore, the prevalence and characteristics of BFS still need to be established. However, among the ...
متن کامل[Amyotrophic lateral sclerosis].
Amyotrophic lateral sclerosis (ALS) is a progressive, degenerative disease of the motor system characterized by signs and symptoms of upper and lower motor dysfunction. This results in the presence of focal amyotrophies and pareses affecting voluntary muscles. Patients die after a few years, in most cases by respiratory failure. ALS is the most frequent motor neuron disease; however, its etiolo...
متن کاملAmyotrophic lateral sclerosis.
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder affecting 20,000 to 30,000 people in the United States. The mainstay of care of patients affected by this disease is supportive and given the multifaceted nature of their needs is provided most efficiently through multidisciplinary clinics that have shown to prolong survival and improve quality of life. The authors ...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: The Egyptian Journal of Neurology, Psychiatry and Neurosurgery
سال: 2023
ISSN: ['1687-8329', '1110-1083']
DOI: https://doi.org/10.1186/s41983-023-00671-1