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The Gaucher Earlier Diagnosis Consensus point-scoring system for children and young adults: a retrospective and prospective evaluation in Korea
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Hahn, Seung Min | - |
| dc.contributor.author | Kim, Minseok | - |
| dc.contributor.author | Kim, Youna | - |
| dc.contributor.author | Oh, Jiyoung | - |
| dc.contributor.author | Kim, Se Hee | - |
| dc.contributor.author | Koh, Hong | - |
| dc.contributor.author | Kim, Sung-Eun | - |
| dc.contributor.author | Chung, Nack-Gyun | - |
| dc.contributor.author | Shim, Ye Jee | - |
| dc.contributor.author | Kim, Hawk | - |
| dc.contributor.author | Lee, Jae Min | - |
| dc.contributor.author | Yoon, Sung-Soo | - |
| dc.contributor.author | Im, Ho Joon | - |
| dc.contributor.author | Kang, Hyoung Jin | - |
| dc.contributor.author | Do, Young Rok | - |
| dc.contributor.author | Nam, Chung Mo | - |
| dc.contributor.author | Lyu, Chuhl Joo | - |
| dc.date.accessioned | 2025-11-18T03:09:35Z | - |
| dc.date.available | 2025-11-18T03:09:35Z | - |
| dc.date.created | 2025-12-11 | - |
| dc.date.issued | 2025-11 | - |
| dc.identifier.issn | 1750-1172 | - |
| dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/209005 | - |
| dc.description.abstract | PurposeGaucher disease (GD) is an autosomal recessive condition caused by insufficient glucocerebrosidase activity. The Gaucher Earlier Diagnosis Consensus (GED-C) initiative created a point-scoring system (PSS) to facilitate the early identification of GD based on significant indicators and covariables. This study aimed to evaluate the applicability and utility of the GED-C PSS in pediatric and young adult patients in Korea.ResultsThis study included both retrospective analysis and prospective recruitment. Subject recruitment involved 14 sites across 13 hospitals in Korea, where patients of any age meeting GED-C criteria were recruited, and blood samples were collected. Data of 513 subjects were analyzed and two patients were confirmed to have GD during prospective enrollment. The median age of participants was 10 years (range: 1 month to 40 years). Receiver operating characteristic analysis revealed a cutoff point of 6.5 for GED-C PSS (area under the curve of 0.9883) demonstrated high sensitivity (1.0) and specificity (0.97). A histogram indicated that the PSS scores of the two confirmed GD patients were distinct from those of other participants.ConclusionsThe study suggests that GED-C PSS shows potential for the early diagnosis of GD, supporting its broader clinical use for both children and adults. | - |
| dc.description.statementOfResponsibility | open | - |
| dc.format | application/pdf | - |
| dc.language | English | - |
| dc.publisher | BioMed Central | - |
| dc.relation.isPartOf | ORPHANET JOURNAL OF RARE DISEASES | - |
| dc.relation.isPartOf | ORPHANET JOURNAL OF RARE DISEASES | - |
| dc.rights | CC BY-NC-ND 2.0 KR | - |
| dc.subject.MESH | Adolescent | - |
| dc.subject.MESH | Adult | - |
| dc.subject.MESH | Child | - |
| dc.subject.MESH | Child, Preschool | - |
| dc.subject.MESH | Early Diagnosis | - |
| dc.subject.MESH | Female | - |
| dc.subject.MESH | Gaucher Disease* / diagnosis | - |
| dc.subject.MESH | Humans | - |
| dc.subject.MESH | Infant | - |
| dc.subject.MESH | Male | - |
| dc.subject.MESH | Prospective Studies | - |
| dc.subject.MESH | Republic of Korea | - |
| dc.subject.MESH | Retrospective Studies | - |
| dc.subject.MESH | Young Adult | - |
| dc.title | The Gaucher Earlier Diagnosis Consensus point-scoring system for children and young adults: a retrospective and prospective evaluation in Korea | - |
| dc.type | Article | - |
| dc.contributor.college | College of Medicine (의과대학) | - |
| dc.contributor.department | Dept. of Pediatrics (소아과학교실) | - |
| dc.contributor.googleauthor | Hahn, Seung Min | - |
| dc.contributor.googleauthor | Kim, Minseok | - |
| dc.contributor.googleauthor | Kim, Youna | - |
| dc.contributor.googleauthor | Oh, Jiyoung | - |
| dc.contributor.googleauthor | Kim, Se Hee | - |
| dc.contributor.googleauthor | Koh, Hong | - |
| dc.contributor.googleauthor | Kim, Sung-Eun | - |
| dc.contributor.googleauthor | Chung, Nack-Gyun | - |
| dc.contributor.googleauthor | Shim, Ye Jee | - |
| dc.contributor.googleauthor | Kim, Hawk | - |
| dc.contributor.googleauthor | Lee, Jae Min | - |
| dc.contributor.googleauthor | Yoon, Sung-Soo | - |
| dc.contributor.googleauthor | Im, Ho Joon | - |
| dc.contributor.googleauthor | Kang, Hyoung Jin | - |
| dc.contributor.googleauthor | Do, Young Rok | - |
| dc.contributor.googleauthor | Nam, Chung Mo | - |
| dc.contributor.googleauthor | Lyu, Chuhl Joo | - |
| dc.identifier.doi | 10.1186/s13023-025-03891-1 | - |
| dc.relation.journalcode | J03433 | - |
| dc.identifier.eissn | 1750-1172 | - |
| dc.identifier.pmid | 41214801 | - |
| dc.subject.keyword | Gaucher disease | - |
| dc.subject.keyword | Lysosomal storage disorder | - |
| dc.subject.keyword | Early diagnosis | - |
| dc.contributor.alternativeName | Lyu, Chuhl Joo | - |
| dc.contributor.affiliatedAuthor | Hahn, Seung Min | - |
| dc.contributor.affiliatedAuthor | Kim, Minseok | - |
| dc.contributor.affiliatedAuthor | Kim, Youna | - |
| dc.contributor.affiliatedAuthor | Oh, Jiyoung | - |
| dc.contributor.affiliatedAuthor | Kim, Se Hee | - |
| dc.contributor.affiliatedAuthor | Koh, Hong | - |
| dc.contributor.affiliatedAuthor | Nam, Chung Mo | - |
| dc.contributor.affiliatedAuthor | Lyu, Chuhl Joo | - |
| dc.identifier.scopusid | 2-s2.0-105021257821 | - |
| dc.identifier.wosid | 001614067200002 | - |
| dc.citation.volume | 20 | - |
| dc.citation.number | 1 | - |
| dc.identifier.bibliographicCitation | ORPHANET JOURNAL OF RARE DISEASES, Vol.20(1), 2025-11 | - |
| dc.identifier.rimsid | 90267 | - |
| dc.type.rims | ART | - |
| dc.description.journalClass | 1 | - |
| dc.description.journalClass | 1 | - |
| dc.subject.keywordAuthor | Gaucher disease | - |
| dc.subject.keywordAuthor | Lysosomal storage disorder | - |
| dc.subject.keywordAuthor | Early diagnosis | - |
| dc.subject.keywordPlus | LYSOSOMAL STORAGE DISORDERS | - |
| dc.subject.keywordPlus | DISEASE | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | Y | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalWebOfScienceCategory | Genetics & Heredity | - |
| dc.relation.journalWebOfScienceCategory | Medicine, Research & Experimental | - |
| dc.relation.journalResearchArea | Genetics & Heredity | - |
| dc.relation.journalResearchArea | Research & Experimental Medicine | - |
| dc.identifier.articleno | 569 | - |
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