DYT21: Late onset dystonia
Evidence-based neurology checklist on dyt21: late onset dystonia: Genetics This is caused by mutations in chromosome 2 The transmission is autosomal dominant It causes late onset dystonia The onset age is 13-50 years: it is usually around 25 years Dystonia phenotypes Treatment
Genetics
- This is caused by mutations in chromosome 2
- The transmission is autosomal dominant
- It causes late onset dystonia
- The onset age is 13-50 years: it is usually around 25 years
Dystonia phenotypes
Treatment
References
- Norgren N, Mattson E, Forsgren L, Holmberg M. A high-penetrance form of late-onset torsion dystonia maps to a novel locus (DYT21) on chromosome 2q14.3-q21.3. Neurogenetics 2011; 12:137-143.
- Forsgren L, Holmgren G, Almay BG, Drugge U. Autosomal dominant torsion dystonia in a Swedish family. Adv Neurol 1988; 50:83-92.
Related checklists
- 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)
- 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