Early-onset autosomal dominant GTP-cyclohydrolase I deficiency: Diagnostic delay and residual motor signs
DC Field | Value | Language |
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dc.contributor.author | Kim, WooJoong | - |
dc.contributor.author | Cho, Jae So | - |
dc.contributor.author | Shim, Young Kyu | - |
dc.contributor.author | Ko, Young Jun | - |
dc.contributor.author | Choi, Sun Ah | - |
dc.contributor.author | Kim, Soo Yeon | - |
dc.contributor.author | Kim, Hunmin | - |
dc.contributor.author | Lim, Byung Chan | - |
dc.contributor.author | Hwang, Hee | - |
dc.contributor.author | Choi, Jieun | - |
dc.contributor.author | Kim, Ki Joong | - |
dc.contributor.author | Kim, Man Jin | - |
dc.contributor.author | Seong, Moon-Woo | - |
dc.contributor.author | Chae, Jong-Hee | - |
dc.date.accessioned | 2024-07-05T02:00:24Z | - |
dc.date.available | 2024-07-05T02:00:24Z | - |
dc.date.issued | 2021-08 | - |
dc.identifier.issn | 0387-7604 | - |
dc.identifier.issn | 1872-7131 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/74601 | - |
dc.description.abstract | Objective: Autosomal dominant (AD) guanosine triphosphate cyclohydrolase 1 (GCH1) deficiency is the most common cause of dopa-responsive dystonia (DRD). Patients with GCH1 deficiency are likely to experience diagnostic delay, but its consequences have not been described thoroughly in patients with early-onset disease. We describe the diagnostic delay and residual motor signs (RMS) observed in patients with early-onset (before 15 years of age) disease. Methods: Twelve patients with early-onset AD GCH1 deficiency from a single center were included in the case series analysis. For the meta-analysis, the PubMed database was searched for articles on early-onset AD GCH1 deficiency published from 1995 to 2019. Results: In the case series, the mean duration of diagnostic delay was 5.6 years. Two patients exhibited RMS, and four patients underwent orthopedic surgery. The literature search yielded 137 AD GCH1 deficiency cases for review; gait disturbance was reported in 92.7% of patients, diurnal fluctuation of symptoms in 91.9%, and RMS in 39%. The mean duration of diagnostic delay was 14.6 years overall: 12.0 years in RMS-negative patients and 21.2 years in RMS-positive patients. Conclusions: Diagnostic delay in early-onset AD GCH1 deficiency is more closely associated with later RMS. Early clinical suspicion, timely diagnosis, and levodopa treatment may reduce the occurrence of RMS in patients with early-onset AD GCH1 deficiency. (c) 2021 Published by Elsevier B.V. on behalf of The Japanese Society of Child Neurology. | - |
dc.format.extent | 9 | - |
dc.language | 영어 | - |
dc.language.iso | ENG | - |
dc.publisher | ELSEVIER | - |
dc.title | Early-onset autosomal dominant GTP-cyclohydrolase I deficiency: Diagnostic delay and residual motor signs | - |
dc.type | Article | - |
dc.identifier.doi | 10.1016/j.braindev.2021.02.006 | - |
dc.identifier.bibliographicCitation | BRAIN & DEVELOPMENT, v.43, no.7, pp 759 - 767 | - |
dc.description.isOpenAccess | N | - |
dc.identifier.wosid | 000663463200003 | - |
dc.identifier.scopusid | 2-s2.0-85104347771 | - |
dc.citation.endPage | 767 | - |
dc.citation.number | 7 | - |
dc.citation.startPage | 759 | - |
dc.citation.title | BRAIN & DEVELOPMENT | - |
dc.citation.volume | 43 | - |
dc.type.docType | Article | - |
dc.publisher.location | 네델란드 | - |
dc.subject.keywordAuthor | Guanosine triphosphate cyclohydrolase 1 | - |
dc.subject.keywordAuthor | Dopa-responsive dystonia | - |
dc.subject.keywordAuthor | Segawa disease | - |
dc.subject.keywordAuthor | Residual motor signs | - |
dc.subject.keywordAuthor | Diagnostic delay | - |
dc.subject.keywordPlus | DOPA-RESPONSIVE DYSTONIA | - |
dc.subject.keywordPlus | HEREDITARY PROGRESSIVE DYSTONIA | - |
dc.subject.keywordPlus | GCH1 GENE | - |
dc.subject.keywordPlus | MISSENSE MUTATION | - |
dc.subject.keywordPlus | HETEROZYGOUS MUTATION | - |
dc.subject.keywordPlus | ATYPICAL PRESENTATION | - |
dc.subject.keywordPlus | CHINESE PATIENTS | - |
dc.subject.keywordPlus | SEGAWA-SYNDROME | - |
dc.subject.keywordPlus | KOREAN FAMILY | - |
dc.subject.keywordPlus | PHENOTYPE | - |
dc.relation.journalResearchArea | Neurosciences & Neurology | - |
dc.relation.journalResearchArea | Pediatrics | - |
dc.relation.journalWebOfScienceCategory | Clinical Neurology | - |
dc.relation.journalWebOfScienceCategory | Pediatrics | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
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