Abstract
Neurofibrillary degeneration (NFD) occurs in the brains of patients with myotonic dystrophy (DM) type 1. The authors report a similar tau pathology in the CNS of a patient with DM2 and compare it to that of patients with DM1. A reduced expression of tau exon 2 and exon 3 epitopes is observed in both DM1 and DM2. This suggests a similar physiopathologic process that may contribute to common neurologic features in patients with DM.
Original language | English (US) |
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Pages (from-to) | 1636-1638 |
Number of pages | 3 |
Journal | Neurology |
Volume | 65 |
Issue number | 10 |
DOIs | |
State | Published - Nov 2005 |
ASJC Scopus subject areas
- Clinical Neurology