Rohani Mohammad, Shahidi Gholamali, Alavi Afagh, Lang Anthony E, Yousefi Niloufar, Razme Said, Fasano Alfonso
Morton and Gloria Shulman Movement Disorders Clinic and the Edmond J. Safra Program in Parkinson's Disease Toronto Western Hospital and Division of Neurology University of Toronto Toronto Ontario Canada.
Department of Neurology Hazrat Rasool Hospital Iran University of Medical Sciences Tehran Iran.
Mov Disord Clin Pract. 2017 Jun 30;4(5):772-774. doi: 10.1002/mdc3.12512. eCollection 2017 Sep-Oct.
Neurodegeneration with brain iron accumulation (NBIA) includes a rare and heterogeneous group of disorders characterized by iron deposition in the basal ganglia. Pantothenate kinase-associated neurodegeneration (PKAN) is the most common NBIA and has 2 main presentations: typical and atypical, the latter rarely presents with tremor. Our reported patients underwent full neurologic examination, standard brain magnetic imaging, and genetic testing for PKAN. Three patients who had "tremor-dominant" PKAN with a relatively benign course were reported, including 1 with dystonic tremor and 2 with parkinsonian tremor. All 3 patients had homozygous mutations in the PANK2 gene and typical eye of the tiger sign on brain imaging. PKAN (and NBIA in general) may be a potential cause of tremor, thus emphasizing the need to consider this diagnosis even in patients with a clinical diagnosis of essential, dystonic, or parkinsonian tremor.
脑铁沉积神经变性病(NBIA)包括一组罕见的异质性疾病,其特征为基底节铁沉积。泛酸激酶相关神经变性病(PKAN)是最常见的NBIA,有两种主要表现形式:典型型和非典型型,后者很少出现震颤。我们报告的患者接受了全面的神经系统检查、标准脑磁共振成像以及PKAN基因检测。报告了3例病程相对良性的“震颤为主型”PKAN患者,其中1例为肌张力障碍性震颤,2例为帕金森震颤。所有3例患者PANK2基因均存在纯合突变,且脑成像有典型的虎眼征。PKAN(以及一般的NBIA)可能是震颤的潜在病因,因此强调即使对于临床诊断为特发性、肌张力障碍性或帕金森震颤的患者,也有必要考虑这一诊断。