| Literature DB >> 31367947 |
Petyo Nikolov1,2, Shady S Hassan2,3, Aykut Aytulun1, Christian J Hartmann1,2, Jürgen Kohlhase4, Alfons Schnitzler1,2, Philipp Albrecht1, Martina Minnerop1,2,5, Stefan Jun Groiss6,7.
Abstract
DYT-THAP1 dystonia is known to present a variety of clinical symptoms. To the best of our knowledge, this is the first case with DYT-THAP 1 dystonia and clinical signs of cerebellar involvement studied with transcranial magnetic stimulation in vivo. We report a case of a 51-year-old male DYT-THAP1 mutation carrier with dystonia, who additionally developed ataxia 1.5 years ago. To study cerebellar involvement in our patient, we used a TMS protocol called cerebellar inhibition (CBI). The lack of CBI in our patient strongly suggests cerebellar involvement. According to our findings, cerebellar syndrome may be part of the phenotypical spectrum of DYT-THAP1 mutations.Entities:
Keywords: Ataxia; DYT-THAP-1; Dystonia; TMS
Mesh:
Substances:
Year: 2019 PMID: 31367947 DOI: 10.1007/s12311-019-01062-0
Source DB: PubMed Journal: Cerebellum ISSN: 1473-4222 Impact factor: 3.847