Sep 2026· TAJ Journal of Teachers Association· Vol 39, pp. 294-300· 0 citations· 13 references
TL;DR
GBS in this Bangladeshi cohort showed mixed electrophysiological patterns, with AIDP predominance and substantial AMAN burden.
Abstract
Background: Guillain-Barré syndrome (GBS) is classified into demyelinating (AIDP) and axonal (AMAN, AMSAN) subtypes by nerve conduction studies, with distinct clinical courses and prognoses. Regional variation in subtype distribution is documented, but Bangladeshi data linking clinical and cerebrospinal fluid (CSF) findings to subtype remain scarce. We aimed to determine the distribution of nerve-conduction-defined subtypes and their associations with demographic, clinical, and CSF characteristics in adults with GBS. Methods: This cross-sectional study was performed at Dhaka Medical College Hospital from November 2013 to November 2014. Fifty people with clinically confirmed Guillain-Barré Syndrome received neurological evaluation, nerve conduction studies, and cerebrospinal fluid analysis at least seven days post-symptom start. Patients were categorised as having acute inflammatory demyelinating polyradiculoneuropathy (AIDP), acute motor axonal neuropathy (AMAN), or acute motor and sensory axonal neuropathy (AMSAN). CSF, neurological, clinical, and demographic characteristics were compared between subgroups. Results: AIDP was the most common subtype, observed in 25 patients (50.0%), followed by AMAN in 21 (42.0%) and AMSAN in 4 (8.0%). Age distribution differed significantly among subtypes (p=0.036), with AMAN more frequent in younger adults and AMSAN more frequent in older patients. Symmetrical ascending weakness was common across subtypes: AIDP 88.0%, AMAN 95.2%, and AMSAN 100.0%. Sensory symptoms and impaired sensory examination were present only in AMSAN and were significantly associated with subtype (both p=0.001). Ventilatory support was numerically highest in AMAN (38.1%). Raised CSF protein was frequent across all subtypes with normal CSF cell counts. CSF protein >170 mg/dL was more common in AIDP than AMAN (88.0% vs 28.6%). Conclusion: GBS in this Bangladeshi cohort showed mixed electrophysiological patterns, with AIDP predominance and substantial AMAN burden. Sensory involvement suggested AMSAN, while CSF supported diagnosis but not subtype classification.
Abstract Background Early European lyme neuroborreliosis (LNB) presents with distinct clinical manifestations, but comparative data on cerebrospinal fluid (CSF) findings across these forms are limited. Methods We conducted a retrospective study of 405 patients with confirmed early LNB treated at a single center between...
K. Ogrinc, P. Bogovič, A. Kastrin et al.· Open Forum Infectious Diseas...· 0 citations
Background: Guillain-Barré syndrome (GBS) is a rare but potentially life-threatening immune-mediated disorder affecting peripheral nerves, causing acute flaccid paralysis with variable clinical severity. Its diverse presentation and disease course make diagnosis, management, and prognostication difficult, particularly...
S. K. Sumi, F. Rashid, M. S. N. Sumi et al.· International Journal of Con...· 0 citations
Advances in serial nerve conduction studies and electrodiagnostic criteria have improved recognition and classification of atypical presentations, including reversible conduction failure, and Parallel developments in clinical assessment and prognostic tools have strengthened prediction of respiratory compromise and fun...
D. Maini· Evolution of Guillain-Barré...· 0 citations
Background Guillain-Barré syndrome (GBS) is an acute immune-mediated polyradiculoneuropathy that may follow infectious triggers and can progress to severe weakness, cranial nerve involvement, autonomic dysfunction, and respiratory failure. Cytomegalovirus (CMV)-associated GBS is often linked to a more severe clinical c...
Alessio D'Elia, Luciana Mascia, L. Giaccari et al.· Frontiers in Immunology· 0 citations
Fulminant bulbar-predominant AMAN may mimic upper-airway pathology and present before CSF protein elevation in this case, and neurological improvement occurred after initiation of plasma exchange and intensive supportive care; however, causality cannot be inferred from a single case.
Ali Al Hassani, Zaid Al Hassani, F. AlKindi et al.· European Journal of Medical...· 0 citations
BACKGROUND
Acute motor and sensory axonal neuropathy is a rare, severe variant of Guillain-Barré syndrome marked by rapid progression, autonomic dysfunction, and delayed recovery. The patient in this report was treated in a resource-limited intensive care unit and had coexisting tropical infections that complicated dia...
Noor Hasmee, Bhupendra Singh, H. Joshi· Critical Care Nurse· 0 citations
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