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Neurofilament light chain (NEFL) 유전자 돌연변이 CMT 환자들의 전기생리학적 특성

Other Titles
 Electrophysiological Characteristics of Charcot-Marie-Tooth Patients with Mutations in Neurofilament Light Chain (NEFL) Gene 
Authors
 조현지  ;  박기덕  ;  서범천  ;  김승민  ;  선우일남  ;  김대성  ;  최병옥 
Citation
 Journal of the Korean Association of EMG-Electrodiagnostic Medicine (대한근전도 전기진단의학회지), Vol.7(2) : 109-117, 2005 
Journal Title
 Journal of the Korean Association of EMG-Electrodiagnostic Medicine (대한근전도 전기진단의학회지) 
ISSN
 1229-6066 
Issue Date
2005
MeSH
Neuropathy ; Charcot-Marie-Tooth disease ; Neurofilament protein L ; Mutation
Keywords
Neuropathy ; Charcot-Marie-Tooth disease ; Neurofilament protein L ; Mutation
Abstract
Objectives: Charcot-Marie-Tooth (CMT) disease is the most common form of hereditary motor and sensory neuropathy. Several genes were recently identified to cause autosomal dominant CMT2 including neurofilament light chain(NEFL) gene. NEFL encodes a 62kDa structural protein, which is one of the most abundant cytoskeletal components of neural cells. CMT with NEFL gene was recently known and there was controversies about the pathogical and electophysiological changes in this disease. Therefore, we investigated to find the pathological and electrophysiological characteristics in Korean CMT patients with NEFL mutation. Methods: Mutations of the NEFL gene were examed in 125 unrelated Korean families diagnosed as having CMT disease, and 105 normal individuals. Nerve conduction studies were carried out all study populations. Results: Three pathogenic mutations (Pro22Arg, Leu334Pro, Glu397Lys) were found in three families (FC#7, 21, 99), respectively. Electrophyiologically, FC#21 patient represented axonal neuropathy (CMT2E), and the others showed demyelinating neuropathy (CMT1). In patient with Leu334Pro mutation, the results of follow-up nerve conduction studies showed very slow disease progress, and pathological findings displayed small loss of large myelinated fibers. Conclusion: NEFL mutations cause both demyelinating and axonal neuropathies. Therefore, analysis of the NEFL gene should not be restricted to pure axonal neuropathy.
Files in This Item:
T200501657.pdf Download
DOI
OAK-2005-06755
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Neurology (신경과학교실) > 1. Journal Papers
Yonsei Authors
Kim, Seung Min(김승민) ORCID logo https://orcid.org/0000-0002-4384-9640
Sunwoo, Il Nam(선우일남)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/149894
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