[Molecular and anatomical bases of dystonia: X-linked recessive dystonia-parkinsonism (DYT3)].

@article{Kaji2005MolecularAA,
  title={[Molecular and anatomical bases of dystonia: X-linked recessive dystonia-parkinsonism (DYT3)].},
  author={Ryuji Kaji and Satoshi Goto and Gen Tamiya and Lillian V. Lee},
  journal={Rinsho shinkeigaku = Clinical neurology},
  year={2005},
  volume={45 11},
  pages={811-4}
}
Pathological findings in dystonia have been unclear. X-linked recessive dystonia-parkinsonism (XDP, DYT3), endemic in the Panay island, the Philippines, is characterized by the clinical onset with dystonia followed by parkinsonism. It provides a unique opportunity to explore the anatomical basis of dystonia, because it has discernible pathological changes… CONTINUE READING