Ocal, Ruhsen2019-06-012019-06-0120172147-2092http://medicaljournal.gazi.edu.tr/index.php/GMJ/article/view/1477http://hdl.handle.net/11727/3369Aim: Wilson's disease (WD) is a hereditary disease that causes the accumulation of copper in many organs and tissues due to impaired copper transport. WD is presented with neurological and neuropsychiatric findings. Prognosis is usually dependent on severity of liver involvement and neurological involvement. Early treatment can control brain damage and symptoms. The time of diagnosis is related to prognosis. Our aim in this study is to determine the frequency of WD neurological manifestations in our clinic and to convey our clinical experience. Methods: Patients with diagnosis of WD and complaints were examined in the neurology outpatient clinic between 2014 and 2017. Clinical and radiological images of the patients were reviewed. Results: A total of 36 patients (11 female, 25 male) were included in the study. In the neurological examination of these patients. Only tremor was found in 4 patients, tremor and dystonia in 2 patients, tremor and chorea in 2 patients, tremor and choreatetosis in 1 patient and epilepsy in 2 patients. Neurological involvement was detected in 30.5 % of 36 WD neurological follow-up patients. Tremor is the most common neurologic finding in patient with involvement of central nervous system in WD. Symptom is tremor with 81.8 % of patients with neurological symptoms. Tremor was detected in 44.4 % of patients with WD, while another 55.6 % were accompanied by another movement disorders. Conclusion: Neurological complications are common in Wilson's disease. The most common symptom seen is tremor.turinfo:eu-repo/semantics/openAccessWilson's diseaseTremorMovement disorderarticle2842572590004180121000072-s2.0-85030622846