Neurology Asia 2019;24(3):255-258

doi:7.2019my0102

Analysis of DYT1 and DYT6 in Thai patients with primary dystonia

Pichet Termsarasab 1 ; Chutima Papsing 1 ; Pirada Witoonpanich 1 ; Teeratorn Pulkes 1

Affiliations

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Keywords

Primary dystonia; DYT1 dystonia; DYT6 dystonia; isolated dystonia; DYT-TOR1A; DYTTHAP1; TOR1A; THAP1

Country

Malaysia

Language

English

Abstract

DYT1 and DYT6 dystonias are the two most common genetic primary dystonias. However, they are rare in the Asian population and have never been reported in Thailand. DYT6 dystonia typically presents with craniosegmental dystonia with speech involvement, whereas DYT1 dystonia typically presents with lower limb dystonia, which tends to become generalized over time. Methods: Blood samples were collected from 14 patients with primary dystonia evaluated in five tertiary hospitals in Thailand. Genotyping of the TOR1A and THAP1 gene was performed. Results: Two patients were found to have a missense mutation, p.M143V (c.427A>G), in exon 3 of the THAP1 gene confirming the diagnosis of DYT6 dystonia. One patient was a woman who developed blepharospasm and lower cranial dystonia at the age of 38 years. Her dystonia spread to the neck and arm six months later. The other patient developed focal hand dystonia at the age of 34 years. The TOR1A mutation was not identified in any of these 14 patients.