A superficial siderosis-related transient focal neurological episode in a patient with Marfan syndrome  

作　　者：Slaven Pikija Eugen Trinka Pfaff Johannes Andreea Toma Mahdi Safdarian 

机构地区：[1]Department of Neurology,Neurocritical Care and Neurorehabilitation,Centre of Cognitive Neuroscience,Christian Doppler University Hospital,Paracelsus Medical University,Salzburg,Member of EpiCARE,Salzburg,Austria [2]Department of Neurology,Christian Doppler University Hospital,Centre of Cognitive Neuroscience,Neuroscience Institute,Paracelsus Medical University,Salzburg,Austria [3]Karl Landsteiner Institute for Neurorehabilitation and Space Neurology,Salzburg,Austria [4]Department of Neuroradiology,Christian Doppler University Hospital,Centre of Cognitive Neuroscience,Neuroradiology Institute,Paracelsus Medical University,Salzburg,Austria

出　　处：《Chronic Diseases and Translational Medicine》2023年第3期269-272,共4页慢性疾病与转化医学（英文版）

摘　　要：To the Editor,Marfan syndrome is an autosomal dominant disorder of connective tissue caused by mutations in the gene encoding a matrix component of microfibrils;fibrillin-1(FBN1),with an incidence of about 1-3 per 10,000 individuals.2.3 Cardinal manifestations include proximal aortic aneurysm,dislocation of the ocular lens,and long-bone overgrowth.Dural ectasia,which is defined as a ballooning or significant widening of the dural sac or neural root sleeves,is also a common finding in these patients,which is reported to present in more than 60%of cases and is considered a major criterion for the clinical diagnosis of this syndrome.

关 键 词：SUPERFICIAL MARFAN BALLOON 

分 类 号：R725.9[医药卫生—儿科]