DYT3: X-linked dystonia (Lubag)
Evidence-based neurology checklist on dyt3: x-linked dystonia (lubag): Genetics This is caused by mutations in the TAF1 gene The transmission is X-linked Clinical features Associated movement disorders Psychiatric features Differential diagnosis Magnetic resonance imaging (MRI) brain Treatment
Genetics
- This is caused by mutations in the TAF1 gene
- The transmission is X-linked
Clinical features
Associated movement disorders
Psychiatric features
Differential diagnosis
Magnetic resonance imaging (MRI) brain
Treatment
References
- Muller U. The monogenic primary dystonias. Brain 2009; 132:2005-2025.
- Albanese A, Asmus F, Bhatia KP, et al. EFNS guidelines on diagnosis and treatment of primary dystonias. Eur J Neurol 2011; 18:5-18.
- Ledoux MS, Dauer WT, Warner TT. Emerging common molecular pathways for primary dystonia. Mov Disord 2013; 28:968-981.
- Müller U. The monogenic primary dystonias. Brain 2009; 132:2005-2025.
- Evidente VG, Advincula J, Esteban R, et al. Phenomenology of "Lubag" or X-linked dystonia-parkinsonism. Mov Disord 2002; 17:1271-1277.
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