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Dopa Responsive Parkinsonism in an Early Onset Alzheimer's Disease Patient with a Presenilin 1 Mutation (A434T)

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dc.contributor.authorJo, Hyunjin-
dc.contributor.authorKim, Minkyeong-
dc.contributor.authorPark, Seongbeom-
dc.contributor.authorPark, Jong Eun-
dc.contributor.authorCho, Soo Hyun-
dc.contributor.authorKim, Seung Joo-
dc.contributor.authorJang, Hyemin-
dc.contributor.authorJung, Yong Hee-
dc.contributor.authorKim, Junpyo-
dc.contributor.authorNa, Duk L.-
dc.contributor.authorSeo, Sang Won-
dc.contributor.authorCho, Jin Whan-
dc.contributor.authorKim, Hee Jin-
dc.date.accessioned2023-09-04T19:14:16Z-
dc.date.available2023-09-04T19:14:16Z-
dc.date.created2023-07-19-
dc.date.issued2019-06-
dc.identifier.issn1387-2877-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/190154-
dc.description.abstractAlzheimer's disease patients with presenilin 1 (PSEN1) mutations commonly show parkinsonism in addition to dementia. Yet, whether these patients show dopaminergic deficit and response to L-dopa is largely unknown. We report a 43-year-old woman with a PSEN1 mutation (A434T) who showed right side dominant parkinsonism. As disease progressed, she developed bilateral parkinsonism which was markedly relieved by L-dopa. Amyloid (Florbetaben) positron-emission tomography (PET) showed cortical florbetaben uptake, relatively sparing the striatum. Initial dopamine transporter (FP-CIT) PET showed asymmetrically decreased FP-CIT uptake in the left striatum. We suggest that in Alzheimer's disease patients with PSEN1 mutation, parkinsonism may be relieved by L-dopa when it is associated with presynaptic dopaminergic deficit.-
dc.language영어-
dc.language.isoen-
dc.publisherIOS PRESS-
dc.titleDopa Responsive Parkinsonism in an Early Onset Alzheimer's Disease Patient with a Presenilin 1 Mutation (A434T)-
dc.typeArticle-
dc.contributor.affiliatedAuthorPark, Jong Eun-
dc.identifier.doi10.3233/JAD-190469-
dc.identifier.scopusid2-s2.0-85071897548-
dc.identifier.wosid000484216500002-
dc.identifier.bibliographicCitationJOURNAL OF ALZHEIMERS DISEASE, v.71, no.1, pp.7 - 13-
dc.relation.isPartOfJOURNAL OF ALZHEIMERS DISEASE-
dc.citation.titleJOURNAL OF ALZHEIMERS DISEASE-
dc.citation.volume71-
dc.citation.number1-
dc.citation.startPage7-
dc.citation.endPage13-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.subject.keywordPlusCLINICAL-FEATURES-
dc.subject.keywordPlusALPHA-SYNUCLEIN-
dc.subject.keywordPlusLEWY BODIES-
dc.subject.keywordPlusDEMENTIA-
dc.subject.keywordPlusPATHOLOGY-
dc.subject.keywordPlusPREVALENCE-
dc.subject.keywordPlusGENETICS-
dc.subject.keywordPlusFAMILY-
dc.subject.keywordAuthorAlzheimer&apos-
dc.subject.keywordAuthors disease-
dc.subject.keywordAuthorFP-CIT PET-
dc.subject.keywordAuthorL-dopa-
dc.subject.keywordAuthorparkinsonism-
dc.subject.keywordAuthorpresenilin 1-
dc.identifier.urlhttps://content.iospress.com/articles/journal-of-alzheimers-disease/jad190469-
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