Abstract
We report five patients with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) who had demyelinating peripheral neuropathy. The MNGIE neuropathy had clinical and electrodiagnostic features typical of acquired, rather than inherited, etiologies. In fact, three patients were actually treated for chronic inflammatory demyelinating polyneuropathy (CIDP). We discuss findings that may help distinguish patients with MNGIE from those with CIDP.
Original language | English (US) |
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Pages (from-to) | 364-368 |
Number of pages | 5 |
Journal | Muscle and Nerve |
Volume | 29 |
Issue number | 3 |
DOIs | |
State | Published - Mar 2004 |
Keywords
- Demyelination
- Inflammation
- Mitochondria
- Mitochondrial myopathy
- Peripheral neuropathy
- Thymidine phosphorylase
ASJC Scopus subject areas
- Physiology
- Clinical Neurology
- Cellular and Molecular Neuroscience
- Physiology (medical)