DYSTONIA neurology checklists
Explore evidence-based neurology topics and fully referenced clinical checklists covering DYSTONIA.
Dystonia: causes and risk factors
Dystonia clinical features
Primary dystonia: DYT1-DYT14
- DYT1: Early onset primary dystonia
- DYT2: Autosomal recessive torsion dystonia
- DYT3: X-linked dystonia (Lubag)
- DYT4: Whispering dysphonia
- DYT5: Dopa-responsive dystonia (DRD): clinical features
- DYT5: Dopa-responsive dystonia (DRD): variants and differentials
- DYT5: Dopa-responsive dystonia (DRD): management
- DYT6: Adult onset mixed torsion dystonia
- DYT7: Focal adult onset torsion dystonia
- DYT8: Paroxysmal non-kinesigenic dyskinesia 1 (PNKD1)
- DYT9: Choreoathetosis/spasticity, episodic (CSE)
- DYT10: Paroxysmal kinesigenic dyskinesia 1 (PKD1)
- DYT11: Myoclonus dystonia: clinical features
- DYT11: Myoclonus dystonia: management
- DYT12: Rapid onset dystonia-parkinsonism (RDP)
- DYT13: Familial cranio-cervical dystonia
- DYT14: Dystonia 14
Primary dystonia: DYT15-DYT35
- DYT15: Myoclonic dystonia 15
- DYT16: Autosomal recessive dystonia-parkinsonism
- DYT17: Early onset autosomal recessive dystonia
- DYT18: Paroxysmal exercise-induced dyskinesia (PED)
- DYT19: Paroxysmal kinesigenic dyskinesia 2 (PKD2)
- DYT20: Paroxysmal non-kinesigenic dyskinesia 2 (PNKD2)
- DYT21: Late onset dystonia
- DYT22: Dystonia 22
- DYT23: Dystonia 23
- DYT24: Dystonia 24
- DYT25: Cervical dystonia with local spread
- DYT26: Myoclonic dystonia 26
- DYT27: Dystonia 27
- DYT28: Dystonia 28
- DYT29: Dystonia 29
- DYT30: Dystonia 30
- DYT31: Dystonia 31
- DYT32: Dystonia 32
- DYT33: Dystonia 33
- DYT34: Dystonia 34
- DYT35: Dystonia 35
Craniocervical dystonia
Hemifacial spasm
Oromandibular dystonia
Other craniocervical dystonias
Neurodegeneration with brain iron accumulation (NBIA)
Wilson's disease
- Wilson’s disease: pathology
- Wilson’s disease: neurological features
- Wilson’s disease: systemic features
- Wilson’s disease: scoring system
- Wilson’s disease: differential diagnosis
- Wilson’s disease: MRI features
- Wilson’s disease: other investigations
- Wilson’s disease: treatment
- Wilson’s disease: monitoring and prognosis
Neuroacanthocytosis
Task specific dystonias
Hypermanganesaemia with dystonia 1 (HMNDYT1)
Miscellaneous dystonias
- Tyrosine hydroxylase deficiency (THD)
- Sepiapterin reductase deficiency (SRD)
- Alternating hemiplegia of childhood (AHC)
- Dystonia deafness syndromes
- Paroxysmal autonomic instability with dystonia (PAID)
- Adult onset lower limb dystonia
- Russell Silver syndrome (RSS)
- Paroxysmal tonic upgaze (PTU)
- Oculogyric crisis (OGC)
- Opisthotonus
