Salari Mehri, Fayyazi Emad, Mirmosayyeb Omid
Isfahan Neurosciences Research Center, Alzahra Research Institute, Isfahan University of Medical Sciences, Isfahan, Iran.
Medical Student Research Committee, Isfahan University of Medical Sciences, Isfahan, Iran.
J Res Med Sci. 2018 Mar 27;23:23. doi: 10.4103/jrms.JRMS_362_16. eCollection 2018.
Wilson disease (WD) is a rare autosomal recessive disorder characterized by excessive copper deposition in the body, principally in the liver and the brain. There is a wide spectrum of clinical presentations, but the most significant and basic symptoms of the disease can be divided into hepatic, neurologic, and psychiatric manifestations. Magnetic resonance imaging (MRI) provides more detailed anatomical information than computed tomography of the brain, especially of the structure of the basal ganglia and brain stem. In this review, we want to evaluate the correlation between MRI findings and clinical features of WD.
威尔逊病（WD）是一种罕见的常染色体隐性疾病，其特征是体内铜过度沉积，主要在肝脏和大脑。临床表现多种多样，但该疾病最显著和基本的症状可分为肝脏、神经和精神方面的表现。磁共振成像（MRI）比脑部计算机断层扫描提供更详细的解剖信息，尤其是基底神经节和脑干的结构。在本综述中，我们旨在评估WD的MRI表现与临床特征之间的相关性。
