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ATP1A2 유전자 변이를 보인 산발반신마비 편두통

Other Titles
 Sporadic Hemiplegic Migraine Presenting ATP1A2 Mutation in Korea 
Authors
 김준호  ;  염정연  ;  김남수  ;  신새암  ;  주민경 
Citation
 Journal of the Korean Neurological Association (대한신경과학회지), Vol.40(1) : 51-54, 2022-02 
Journal Title
Journal of the Korean Neurological Association(대한신경과학회지)
ISSN
 1225-7044 
Issue Date
2022-02
Keywords
Sporadic hemiplegic migraine ; ATP1A2 ; Migraine
Abstract
Hemiplegic migraine (HM) is a rare form of migraine, characterized by migraine with reversible motor weakness. HM can be divided into sporadic and familiar HM based on familiarity. Mutations in CACNA1A, ATP1A2 and SCN1A were identified in familiar HM. We present a patient with sporadic HM exhibiting recurrent hemiplegia, mental change and fever along with headache attacks. During the hemiplegia, he showed perfusion delay in left middle cerebral artery territory. Genetic panel test revealed a likely pathogenic varia nt in ATP1A2.
Files in This Item:
T202200771.pdf Download
DOI
10.17340/jkna.2022.1.7
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Laboratory Medicine (진단검사의학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Neurology (신경과학교실) > 1. Journal Papers
Yonsei Authors
Shin, Saeam(신새암) ORCID logo https://orcid.org/0000-0003-1501-3923
Chu, Min Kyung(주민경) ORCID logo https://orcid.org/0000-0001-6221-1346
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/188294
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