Electrodiagnostic findings in myotonic dystrophy: A study on 12 patients
Myotonic dystrophy (DM) is a complex multisystem disease with specific clinical and electrodiagnostic findings. Myotonia can be seen in the distal and proximal muscle groups in upper and lower limbs. There is no established guideline to demonstrate the sensitivity of muscles in the diagnosis of myo...
Main Author: | Ahmet S. Burakgazi |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2019-12-01
|
Series: | Neurology International |
Subjects: | |
Online Access: | https://www.pagepress.org/journals/index.php/ni/article/view/8205 |
Similar Items
-
Core Clinical Phenotypes in Myotonic Dystrophies
by: Stephan Wenninger, et al.
Published: (2018-05-01) -
Electrophysiological evaluation in myotonic dystrophy: correlation with CTG length expansion
by: Pfeilsticker Beatriz Helena Miranda, et al.
Published: (2001-01-01) -
Myotonic Dystrophy Type 1 Associating Sensitive Polyneuropathy: a Case Report
by: Elena Florentina MARINGICA, et al.
Published: (2020-03-01) -
Genotype-Phenotype Correlations and Characterization of Medication Use in Inherited Myotonic Disorders
by: Alayne P. Meyer, et al.
Published: (2020-06-01) -
A Patient with Myotonic Dystrophy Type 1 Presenting as Parkinsonism
by: Ji-Hyun Choi, et al.
Published: (2018-09-01)