Cited 5 times in
Clinical and Pathologic Findings of Korean Patients with RYR1-Related Congenital Myopathy
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 김세훈 | - |
dc.contributor.author | 김승민 | - |
dc.contributor.author | 신하영 | - |
dc.contributor.author | 이정환 | - |
dc.contributor.author | 정하늘 | - |
dc.contributor.author | 최영철 | - |
dc.date.accessioned | 2018-08-28T16:44:15Z | - |
dc.date.available | 2018-08-28T16:44:15Z | - |
dc.date.issued | 2018 | - |
dc.identifier.issn | 1738-6586 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/161888 | - |
dc.description.abstract | BACKGROUND AND PURPOSE: This study was designed to investigate clinical and pathologic characteristics of five Korean patients with RYR1-related congenital myopathy (CM). METHODS: Five patients from unrelated families were diagnosed with RYR1-related CM via direct or targeted sequencing of RYR1. Their clinical, mutational, and pathologic findings were then analyzed. RESULTS: Seven different mutations were identified, including two novel mutations: c.5915A>T and c.12250C>T. All of the patients presented at infancy with proximal dominant weakness and delayed motor milestones. Other clinical findings were scoliosis in three patients, winged scapula in two, hip dislocation in one, and pectus excavatum in one. Ophthalmoplegia was observed in one patient with a novel recessive mutation. Two of three muscle specimens revealed a myopathic pattern with core. CONCLUSIONS: We have identified a novel compound heterozygous RYR1 mutation and demonstrated clinical and pathologic findings in five Korean patients with RYR1-related CM. | - |
dc.description.statementOfResponsibility | open | - |
dc.language | English | - |
dc.publisher | Korean Neurological Association | - |
dc.relation.isPartOf | JOURNAL OF CLINICAL NEUROLOGY | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.rights | https://creativecommons.org/licenses/by-nc-nd/2.0/kr/ | - |
dc.title | Clinical and Pathologic Findings of Korean Patients with RYR1-Related Congenital Myopathy | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine | - |
dc.contributor.department | Dept. of Pathology | - |
dc.contributor.googleauthor | Ha Neul Jeong | - |
dc.contributor.googleauthor | Hyung Jun Park | - |
dc.contributor.googleauthor | Jung Hwan Lee | - |
dc.contributor.googleauthor | Ha Young Shin | - |
dc.contributor.googleauthor | Se Hoon Kim | - |
dc.contributor.googleauthor | Seung Min Kim | - |
dc.contributor.googleauthor | Young Chul Choi | - |
dc.identifier.doi | 10.3988/jcn.2018.14.1.58 | - |
dc.contributor.localId | A00610 | - |
dc.contributor.localId | A00653 | - |
dc.contributor.localId | A02170 | - |
dc.contributor.localId | A03133 | - |
dc.contributor.localId | A05515 | - |
dc.contributor.localId | A04116 | - |
dc.relation.journalcode | J01327 | - |
dc.identifier.eissn | 2005-5013 | - |
dc.identifier.pmid | 29629541 | - |
dc.subject.keyword | RYR1 | - |
dc.subject.keyword | central core disease | - |
dc.subject.keyword | myopathy | - |
dc.subject.keyword | ryanodine receptor 1 | - |
dc.contributor.alternativeName | Kim, Se Hoon | - |
dc.contributor.alternativeName | Kim, Seung Min | - |
dc.contributor.alternativeName | Shin, Ha Young | - |
dc.contributor.alternativeName | Lee, Jung Hwan | - |
dc.contributor.alternativeName | Jeong, Ha Neul | - |
dc.contributor.alternativeName | Choi, Young Chul | - |
dc.contributor.affiliatedAuthor | Kim, Se Hoon | - |
dc.contributor.affiliatedAuthor | Kim, Seung Min | - |
dc.contributor.affiliatedAuthor | Shin, Ha Young | - |
dc.contributor.affiliatedAuthor | Lee, Jung Hwan | - |
dc.contributor.affiliatedAuthor | Jeong, Ha Neul | - |
dc.contributor.affiliatedAuthor | Choi, Young Chul | - |
dc.citation.volume | 14 | - |
dc.citation.number | 1 | - |
dc.citation.startPage | 58 | - |
dc.citation.endPage | 65 | - |
dc.identifier.bibliographicCitation | JOURNAL OF CLINICAL NEUROLOGY, Vol.14(1) : 58-65, 2018 | - |
dc.identifier.rimsid | 59479 | - |
dc.type.rims | ART | - |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.