Clinical Manifestation and Prognosis of Overlapping Acute Motor Axonal Neuropathy and Acute Transverse Myelitis with Anti-GM1 and Anti-GD1a Antibodies: A Case Study

Antibodies against GM1 and GD1a are closely associated with acute motor axonal neuropathy (AMAN). Patients simultaneously positive for both anti-GM1 and anti-GD1a antibodies are rare, and their clinical manifestations and prognosis remain unclear. Herein we report a 41-year-old male diagnosed with AMAN and acute transverse myelitis who was positive for immunoglobulin M anti-GM1, immunoglobulin G (IgG) anti-GM1, and IgG anti-GD1a antibodies. He experienced rapid progression of motor weakness to near quadriplegia within a few days, followed by substantial improvement over 6 months after initiation of steroid treatment, resulting in return of most activities of daily living.

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Publication Details

Journal
Journal of Multiple Sclerosis and Neuroimmunology
Published
2025-06-30
DOI
https://doi.org/10.59578/jmsni.2025.16.1.26-32
Primary Topic
Peripheral Neuropathies and Disorders
Type
article
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article

Clinical Manifestation and Prognosis of Overlapping Acute Motor Axonal Neuropathy and Acute Transverse Myelitis with Anti-GM1 and Anti-GD1a Antibodies: A Case Study

Hyuk Sung Kwon, Jihyoun Jeon, A Young Kim, Heon Yoo
Journal of Multiple Sclerosis and Neuroimmunology
Peripheral Neuropathies and Disorders
article

Clinical Manifestation and Prognosis of Overlapping Acute Motor Axonal Neuropathy and Acute Transverse Myelitis with Anti-GM1 and Anti-GD1a Antibodies: A Case Study

Hyuk Sung Kwon, Jihyoun Jeon, A Young Kim, Heon Yoo
article en

Abstract

Antibodies against GM1 and GD1a are closely associated with acute motor axonal neuropathy (AMAN). Patients simultaneously positive for both anti-GM1 and anti-GD1a antibodies are rare, and their clinical manifestations and prognosis remain unclear. Herein we report a 41-year-old male diagnosed with AMAN and acute transverse myelitis who was positive for immunoglobulin M anti-GM1, immunoglobulin G (IgG) anti-GM1, and IgG anti-GD1a antibodies. He experienced rapid progression of motor weakness to near quadriplegia within a few days, followed by substantial improvement over 6 months after initiation of steroid treatment, resulting in return of most activities of daily living.

Journal of Multiple Sclerosis and NeuroimmunologyVol. 16(1)
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Peripheral Neuropathies and Disorders
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Clinical Manifestation and Prognosis of Overlapping Acute Motor Axonal Neuropathy and Acute Transverse Myelitis with Anti-GM1 and Anti-GD1a Antibodies: A Case Study — Hyuk Sung Kwon, Jihyoun Jeon, et al. · Journal of Multiple Sclerosis and Neuroimmunology (2025) | TGRS Research Map | TGRS