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Autoimmune GFAP Astrocytopathy-Beyond the Known Horizon, India's First Multifaceted Institutional Experience.
Safwan Ahmed1, Vimala Christina Colaco K1, Sudheeran Kannoth2
1Department of Neurology, Father Muller Medical College Hospital, Mangalore, Karnataka, India.
Annals of Neurosciences
|November 15, 2024
Summary
Autoimmune GFAP astrocytopathy presents with diverse neurological symptoms. This first Indian case series highlights varied presentations and a favorable response to treatment, emphasizing diagnostic challenges.
Area of Science:
- Neurology
- Immunology
- Neuroinflammation
Background:
- Autoimmune glial fibrillary acidic protein (GFAP) astrocytopathy is an immune-mediated central nervous system disorder.
- It presents with a wide range of neurological symptoms including meningoencephalitis, myelitis, and seizures.
- Limited literature and no Indian case series exist for this condition.
Purpose of the Study:
- To describe the varied clinical presentations of anti-GFAP astrocytopathy.
- To review the existing literature on autoimmune GFAP astrocytopathy.
- To report the first case series from India.
Main Methods:
- Retrospective study of patients testing positive for GFAP immunoglobulin G in CSF and/or serum.
- Data collected from February 2023 to August 2023.
- Descriptive analysis of clinical and demographic data, with literature review.
Main Results:
- Four patients (3 female:1 male, median age 28) were included.
- Clinical spectrum included ataxia, seizures, myelitis, and autonomic dysfunction.
- All patients responded well to steroids; two received rituximab.
Conclusions:
- Autoimmune GFAP astrocytopathy has an expanding clinical spectrum and should be considered in various neurological disorders.
- The first Indian case series shows a favorable clinical profile.
- Diagnostic challenges highlight the need for a predictive diagnostic algorithm.
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