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深部脑刺激作为早发性泛酸激酶相关神经变性的一种治疗方式。

Deep brain stimulation as a mode of treatment of early onset pantothenate kinase-associated neurodegeneration.

作者信息

Mikati Mohamad A, Yehya Amin, Darwish Houssein, Karam Pascale, Comair Youssef

机构信息

Department of Pediatrics and Adolescent Medicine, American University of Beirut Medical Center, Beirut, Lebanon.

出版信息

Eur J Paediatr Neurol. 2009 Jan;13(1):61-4. doi: 10.1016/j.ejpn.2008.01.006. Epub 2008 May 6.

Abstract

We report a case of a young girl with early onset pantothenate kinase-kssociated neurodegeneration (PKAN) whose initial clinical manifestation was ataxia at the age of 2.5 years. Subsequently the patient presented to us with refractory severe dystonia resulting in essentially complete loss of motor control. She had a mutation in PANK2 gene consisting of an aminoacid change of Alanine to Valine in exon 5 (A382V). After Globus Pallidus deep brain stimulation (DBS) at the age of 11 years, the patient regained useful motor function and speech with a marked decrease in the severity of the dystonia. The patient's condition gradually returned to her pre-DBS status when the device had to be removed 3 months later due to infection. Our case is the sixth case with classical PKAN that was treated by Globus Pallidus stimulation, the fifth one to have a favorable response to it and the only one in whom response was proven by the inadvertent removal of the DBS device due to infection. In addition, our case had a novel mutation and novel clinical features (onset with ataxia, occurrence of early seizure activity) on top of her other symptoms that were otherwise typical of early onset disease.

摘要

我们报告了一例患有早发性泛酸激酶相关神经变性(PKAN)的年轻女孩病例,其最初临床表现为2.5岁时出现共济失调。随后,该患者因难治性严重肌张力障碍前来就诊,导致运动控制基本完全丧失。她的PANK2基因存在突变,外显子5中发生了丙氨酸到缬氨酸的氨基酸变化(A382V)。11岁时接受苍白球深部脑刺激(DBS)后,患者恢复了有用的运动功能和言语能力,肌张力障碍的严重程度显著降低。3个月后,由于感染不得不取出该装置,患者的病情逐渐恢复到DBS治疗前的状态。我们的病例是第六例接受苍白球刺激治疗的经典PKAN病例,是第五例对此有良好反应的病例,也是唯一一例因感染意外取出DBS装置而证实有反应的病例。此外,我们的病例除了具有早发性疾病的其他典型症状外,还具有新的突变和新的临床特征(共济失调起病、早期癫痫活动发作)。

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