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A Practical Guide for Diagnostic Investigations and Special Considerations in Patients With Huntington's Disease in Korea

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dc.contributor.authorMoon, Jangsup-
dc.contributor.authorOh, Eungseok-
dc.contributor.authorKim, Minkyeong-
dc.contributor.authorKim, Ryul-
dc.contributor.authorYoo, Dallah-
dc.contributor.authorShin, Chaewon-
dc.contributor.authorLee, Jee-Young-
dc.contributor.authorKim, Jong-Min-
dc.contributor.authorKoh, Seong-Beom-
dc.contributor.authorKim, Manho-
dc.contributor.authorJeon, Beomseok-
dc.date.accessioned2025-03-12T06:00:17Z-
dc.date.available2025-03-12T06:00:17Z-
dc.date.issued2025-01-
dc.identifier.issn2005-940X-
dc.identifier.issn2093-4939-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/77389-
dc.description.abstractThis review provides a comprehensive framework for the diagnostic approach and management of Huntington's disease (HD) tailored to the Korean population. Key topics include genetic counseling, predictive testing, and reproductive options like preimplantation genetic testing. Strategies for assessing disease progression in premanifest HD through laboratory investigations, biofluid, and imaging biomarkers are highlighted. Special considerations for juvenile and late-onset HD, along with associated comorbidities like diabetes mellitus, hypertension, and cardiovascular abnormalities, are discussed. The guide emphasizes personalized symptom management, including pharmacotherapy, physical therapy, and nutritional support, while exploring emerging disease-modifying treatments. A multidisciplinary care model is advocated to improve outcomes for HD patients and caregivers in Korea.-
dc.format.extent14-
dc.language영어-
dc.language.isoENG-
dc.publisher대한파킨슨병및이상운동질환학회-
dc.titleA Practical Guide for Diagnostic Investigations and Special Considerations in Patients With Huntington's Disease in Korea-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.doi10.14802/jmd.24232-
dc.identifier.scopusid2-s2.0-105000354789-
dc.identifier.wosid001425506600002-
dc.identifier.bibliographicCitationJournal Of Movement Disorders, v.18, no.1, pp 17 - 30-
dc.citation.titleJournal Of Movement Disorders-
dc.citation.volume18-
dc.citation.number1-
dc.citation.startPage17-
dc.citation.endPage30-
dc.type.docTypeReview-
dc.identifier.kciidART003169819-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskciCandi-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalWebOfScienceCategoryClinical Neurology-
dc.subject.keywordPlusREDUCED CANCER INCIDENCE-
dc.subject.keywordPlusCAG-REPEAT LENGTH-
dc.subject.keywordPlusAGE-OF-ONSET-
dc.subject.keywordPlusCOGNITIVE IMPAIRMENT-
dc.subject.keywordPlusPHARMACOLOGICAL-TREATMENT-
dc.subject.keywordPlusCLINICAL PRESENTATION-
dc.subject.keywordPlusDIABETES-MELLITUS-
dc.subject.keywordPlusNATURAL-HISTORY-
dc.subject.keywordPlusJUVENILE-ONSET-
dc.subject.keywordPlusPPAR-GAMMA-
dc.subject.keywordAuthorHuntington's disease-
dc.subject.keywordAuthorGenetic counseling-
dc.subject.keywordAuthorLaboratory investigations-
dc.subject.keywordAuthorBiomarker-
dc.subject.keywordAuthorPremanifest-
dc.subject.keywordAuthorComorbidities-
dc.subject.keywordAuthorManagement-
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