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A Case of Early-Onset Alzheimer's Disease Mimicking Schizophrenia in a Patient with Presenilin 1 Mutation (S170P)

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dc.contributor.authorKim, Hang-Rai-
dc.contributor.authorJang, Ja Hyun-
dc.contributor.authorHam, Honggi-
dc.contributor.authorChoo, Seung Ho-
dc.contributor.authorPark, Jeongho-
dc.contributor.authorKang, Sung Hoon-
dc.contributor.authorHwangbo, Song-
dc.contributor.authorJang, Hyemin-
dc.contributor.authorNa, Duk L.-
dc.contributor.authorSeo, Sang Won-
dc.contributor.authorBaek, Ji Hyun-
dc.contributor.authorKim, Hee Jin-
dc.date.accessioned2022-03-11T23:40:29Z-
dc.date.available2022-03-11T23:40:29Z-
dc.date.created2022-01-20-
dc.date.issued2021-
dc.identifier.issn1387-2877-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/138653-
dc.description.abstractAtypical psychological symptoms frequently occur in early-onset Alzheimer's disease (EOAD), which makes it difficult to differentiate it from other psychiatric disorders. We report the case of a 28-year-old woman with EOAD, carrying a presenilin-1 mutation (S170P), who was initially misdiagnosed with schizophrenia because of prominent psychiatric symptoms in the first 1-2 years of the disease. Amyloid-beta positron emission tomography (PET) showed remarkably high tracer uptake in the striatum and thalamus. Tau PET showed widespread cortical uptake and relatively low uptake in the subcortical and medial temporal regions. Our case advocates for considering EOAD diagnosis for young patients with psychiatric and atypical cognitive symptoms.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherIOS PRESS-
dc.subjectDE-NOVO MUTATION-
dc.subjectNEUROPSYCHIATRIC SYMPTOMS-
dc.subjectCOGNITIVE IMPAIRMENT-
dc.subjectAMYLOID DEPOSITION-
dc.subjectTAU-
dc.subjectNEUROPATHOLOGY-
dc.subjectHETEROGENEITY-
dc.subjectPHENOTYPE-
dc.subjectFREQUENCY-
dc.subjectPSYCHOSIS-
dc.titleA Case of Early-Onset Alzheimer's Disease Mimicking Schizophrenia in a Patient with Presenilin 1 Mutation (S170P)-
dc.typeArticle-
dc.contributor.affiliatedAuthorKang, Sung Hoon-
dc.identifier.doi10.3233/JAD-210650-
dc.identifier.scopusid2-s2.0-85116412294-
dc.identifier.wosid000703410000007-
dc.identifier.bibliographicCitationJOURNAL OF ALZHEIMERS DISEASE, v.83, no.3, pp.1025 - 1031-
dc.relation.isPartOfJOURNAL OF ALZHEIMERS DISEASE-
dc.citation.titleJOURNAL OF ALZHEIMERS DISEASE-
dc.citation.volume83-
dc.citation.number3-
dc.citation.startPage1025-
dc.citation.endPage1031-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.subject.keywordPlusDE-NOVO MUTATION-
dc.subject.keywordPlusNEUROPSYCHIATRIC SYMPTOMS-
dc.subject.keywordPlusCOGNITIVE IMPAIRMENT-
dc.subject.keywordPlusAMYLOID DEPOSITION-
dc.subject.keywordPlusTAU-
dc.subject.keywordPlusNEUROPATHOLOGY-
dc.subject.keywordPlusHETEROGENEITY-
dc.subject.keywordPlusPHENOTYPE-
dc.subject.keywordPlusFREQUENCY-
dc.subject.keywordPlusPSYCHOSIS-
dc.subject.keywordAuthorAlzheimer&apos-
dc.subject.keywordAuthors disease-
dc.subject.keywordAuthorpositron emission tomography-
dc.subject.keywordAuthorPSEN1 mutation-
dc.subject.keywordAuthorpsychosis-
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