Abstract
We systematically evaluated the frequency of neurological disorders and muscle and neural autoantibodies in 177 patients with neuromyelitis optica (NMO) and in 250 control subjects (173 healthy; 77 multiple sclerosis, MS, patients). An excess of myasthenia gravis (MG, 2%), and muscle-type acetylcholine receptor antibody (11%) was detected among NMO patients. The presence of neural or muscle autoantibodies was more common in NMO patients (34%) than in MS patients or healthy controls (7%), P < 0.0001. The coexistence of NMO and MG should be considered in atypical or refractory presentations of either disorder.
Original language | English (US) |
---|---|
Pages (from-to) | 87-90 |
Number of pages | 4 |
Journal | Muscle and Nerve |
Volume | 39 |
Issue number | 1 |
DOIs | |
State | Published - Jan 2009 |
Keywords
- Acetylcholine receptor
- Aquaporin-4
- Autoantibodies
- Multiple sclerosis
- Muscle
- Myasthenia gravis
- Neural
- Neuromyelitis optica
- Water channel
ASJC Scopus subject areas
- Physiology
- Clinical Neurology
- Cellular and Molecular Neuroscience
- Physiology (medical)