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Objectives: Guillain-Barré syndrome (GBS) involves the peripheral nervous system developed by infections or immune conditions. Cerebrospinal fluid (CSF) analysis and electrodiagnostic tests are essential diagnostic methods for GBS. However, limited data are available on how the findings from these methods relate to each other. This study aimed to evaluate changes in CSF analysis and electrodiagnostic tests in pediatrics with GBS.
Materials & Methods: The present study retrospectively evaluated electrodiagnostic tests and CSF changes in pediatrics with GBS who were admitted to Tabriz Hospital, Iran, from 2010 to 2020 due to CBS. Patients' data, including age, gender, CSF analysis, and electrodiagnostic test results, were recorded from the patients' files. Electrodiagnostic data included pace and amplitude of tibial, median, peroneal, sural, ulnar nerves, nerve conduction velocity (NCV), F-wave, and motor unit action potential (MUAP). The significance level was considered less than 0.05.
Results: The mean age of patients was 4.83±2.72 years, and 54.6% were boys. The most common type of GBS involvement was demyelinating type. No gender differences were found between involved nerves unless the ulnar nerve was significantly more involved in girls (P-value: 0.012). The obtained findings indicated no significant relationship between electrodiagnostic tests and CSF protein (P-value: 0.439).
Conclusion: No association was observed between electrodiagnostic results and CSF changes in pediatrics with GBS.
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http://dx.doi.org/10.22037/ijcn.v19i1.44703 | DOI Listing |
J Clin Neuromuscul Dis
September 2025
Centre for Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, United Kingdom; and.
Objectives: X-linked Charcot-Marie-Tooth disease Type 1 (CMTX1), caused by gap junction beta-1 (GJB1) mutations, is the second most common form of CMT. Patients present with length-dependent sensorimotor polyneuropathy and split hand syndrome. Males are more severely affected; females show variable symptoms because of skewed X-inactivation.
View Article and Find Full Text PDFJ Clin Neuromuscul Dis
September 2025
Associated Professor of Radiology, Mashhad University of Medical Sciences, Mashhad, Iran.
A 19-year-old woman presented with acute progressive generalized limb weakness and inability to ambulate, after a recent upper respiratory tract infection. Given the flaccid quadriparesis and preceding infection, Guillain-Barré syndrome (GBS) was initially considered. This case aims to illustrate the diagnostic challenges and the critical role of backward reasoning in differentiating GBS mimickers.
View Article and Find Full Text PDFBMC Neurol
August 2025
Department of Neurology, University of California, San Francisco, USA.
Background: Adult botulism is a rare, life-threatening condition typically caused by exposure to preformed botulinum neurotoxin (BoNT). Acute intestinal toxemia botulism (AITB) is an uncommon subtype resulting from colonization of Clostridium botulinum in the intestines. Diagnosis is made by detecting BoNT in the patient's blood, stool, or gastric fluid.
View Article and Find Full Text PDFJ Neurol
August 2025
Department of Neurology, Rambam Health Care Campus, Haifa, Israel.
Background And Objectives: Accurate interpretation of electrodiagnostic (EDX) studies is essential for the diagnosis and management of neuromuscular disorders. Artificial intelligence (AI) based tools may improve consistency and quality of EDX reporting and reduce workload. The aim of this study is to evaluate the performance of an AI-assisted, multi-agent framework (INSPIRE) in comparison with standard physician interpretation in a randomized controlled trial (RCT).
View Article and Find Full Text PDFJ Peripher Nerv Syst
September 2025
Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Background: Neurofilament light chain (Nf-L) has been identified as a biomarker of neurodegeneration in many neuromuscular conditions, including several subtypes of polyneuropathies. The purpose of this research was to investigate whether Nf-L is also a promising biomarker for idiopathic peripheral neuropathy (IPN), the second most common subtype of axonal polyneuropathy.
Methods: Nf-L levels were quantified using an ultrasensitive digital immunoassay SiMoA in plasma samples from 294 subjects.