Abstract
This review is designed to provide practical help for the clinical neurologist to make appropriate use of the possibilities of molecular diagnosis of inherited movement disorders. Huntington's disease, Parkinson's disease and parkinsonian syndromes, ataxias, Wilson disease, essential tremor, dystonias, and other genetic diseases associated with a variety of movement disorders are considered separately.
Original language | English |
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Pages (from-to) | 3-18 |
Number of pages | 16 |
Journal | Movement Disorders |
Volume | 18 |
Issue number | 1 |
DOIs | |
State | Published - Jan 2003 |
Externally published | Yes |
Keywords
- Autosomal dominant cerebellar ataxias
- Autosomal recessive ataxias
- Essential tremor
- Genetic testing
- Huntington's disease
- Parkinson's disease
- Parkinsonism
- Primary torsion dystonia
- Wilson disease