000020486 001__ 20486
000020486 005__ 20210129210748.0
000020486 0247_ $$2pmid$$apmid:22086712
000020486 0247_ $$2DOI$$a10.1055/s-0031-1281642
000020486 0247_ $$2WOS$$aWOS:000300753900012
000020486 0247_ $$2altmetric$$aaltmetric:459209
000020486 037__ $$aPreJuSER-20486
000020486 041__ $$ager
000020486 082__ $$a610
000020486 084__ $$2WoS$$aClinical Neurology
000020486 084__ $$2WoS$$aPsychiatry
000020486 1001_ $$0P:(DE-HGF)0$$aLehnhardt, F.G.$$b0
000020486 245__ $$aDas psychosoziale Funktionsniveau spätdiagnostizierter PatientInnen mit hochfunktionalem Autismus im Erwachsenenalter.
000020486 260__ $$aStuttgart [u.a.]$$bThieme$$c2012
000020486 300__ $$a88 - 97
000020486 3367_ $$0PUB:(DE-HGF)16$$2PUB:(DE-HGF)$$aJournal Article
000020486 3367_ $$2DataCite$$aOutput Types/Journal article
000020486 3367_ $$00$$2EndNote$$aJournal Article
000020486 3367_ $$2BibTeX$$aARTICLE
000020486 3367_ $$2ORCID$$aJOURNAL_ARTICLE
000020486 3367_ $$2DRIVER$$aarticle
000020486 440_0 $$018781$$aFortschritte der Neurologie  Psychiatrie$$v80$$x0720-4299$$y2
000020486 500__ $$aRecord converted from VDB: 12.11.2012
000020486 520__ $$aThe first time diagnosis of autism spectrum disorder (ASD) after passing childhood and adolescence is still considered a rare event. However, in recent years an increasing demand for diagnostic clarifications with suspected ASD in adulthood challenges this view. There is insufficient knowledge about the neuropsychological characterisation and psychosocial outcome of this adult subgroup in the autistic spectrum.To determine the psychosocial functioning (living status, partnerships, level of education, psychiatric history) of adult patients with late diagnosed ASD.In a retrospective study, a chart review was conducted on 178 consecutively diagnosed individuals at a specialised outpatient clinic for adults with ASD. Global ratings of psychosocial functioning, assessment of psychiatric history and neuropsychological and psychopathological investigations were evaluated.The majority of patients (92 %) diagnosed with ASD suffered from high-functioning autism (HFA)/Asperger syndrome (AS) according to the criteria of ICD-10 (F84.5). The gender ratio was 2:1 favouring males. Mean age at diagnosis (34.1 ± 9.5 years), general intelligence (HAWIE-R, global-IQ 115 ± 20) and self-rated autistic symptoms (autism spectrum quotient [AQ] 39 ± 6) were not discriminative to gender. The psychiatric history revealed a lifetime consultation rate of 78 %, most frequently with depression (50 %). The self-report instrument Beck depression inventory (BDI) identified 30 % of individuals presenting with depressive symptoms in clinical relevant intensity (BDI > 17). Achievement of an independent living status was reported by 68 % of individuals, 58 % reported about current or past intimate partnerships and almost two-thirds of the patients had achieved a higher educational status.The majority of ASD diagnosed late in lifetime turned out to be HFA/AS, presenting with high psychosocial adjustment with regard to independent living, educational status and partnerships. The high level of global intelligence supports the hypothesis of cognitively compensated autistic disturbances leading to the diagnosis comparably late in lifetime. The lifetime rate of psychiatric consultations is high, reflecting the importance to consider a diagnosis of ASD even late in life.
000020486 536__ $$0G:(DE-Juel1)FUEK409$$2G:(DE-HGF)$$aFunktion und Dysfunktion des Nervensystems (FUEK409)$$cFUEK409$$x0
000020486 536__ $$0G:(DE-HGF)POF2-89572$$a89572 - (Dys-)function and Plasticity (POF2-89572)$$cPOF2-89572$$fPOF II T$$x1
000020486 588__ $$aDataset connected to Web of Science, Pubmed
000020486 650_2 $$2MeSH$$aAdult
000020486 650_2 $$2MeSH$$aAge Factors
000020486 650_2 $$2MeSH$$aAsperger Syndrome: psychology
000020486 650_2 $$2MeSH$$aChild
000020486 650_2 $$2MeSH$$aChild Development Disorders, Pervasive: epidemiology
000020486 650_2 $$2MeSH$$aChild Development Disorders, Pervasive: psychology
000020486 650_2 $$2MeSH$$aComorbidity
000020486 650_2 $$2MeSH$$aDepression: complications
000020486 650_2 $$2MeSH$$aDepression: psychology
000020486 650_2 $$2MeSH$$aEducational Status
000020486 650_2 $$2MeSH$$aFemale
000020486 650_2 $$2MeSH$$aHumans
000020486 650_2 $$2MeSH$$aInternational Classification of Diseases
000020486 650_2 $$2MeSH$$aInterpersonal Relations
000020486 650_2 $$2MeSH$$aMale
000020486 650_2 $$2MeSH$$aMental Disorders: etiology
000020486 650_2 $$2MeSH$$aMental Disorders: psychology
000020486 650_2 $$2MeSH$$aMiddle Aged
000020486 650_2 $$2MeSH$$aNeuropsychological Tests
000020486 650_2 $$2MeSH$$aOutpatients
000020486 650_2 $$2MeSH$$aPsychiatric Status Rating Scales
000020486 650_2 $$2MeSH$$aRetrospective Studies
000020486 650_2 $$2MeSH$$aSex Factors
000020486 650_2 $$2MeSH$$aSocial Behavior
000020486 650_2 $$2MeSH$$aYoung Adult
000020486 650_7 $$2WoSType$$aJ
000020486 65320 $$2Author$$aAsperger syndrome
000020486 65320 $$2Author$$aadulthood
000020486 65320 $$2Author$$adiagnosis late in life
000020486 65320 $$2Author$$apsychosocial functioning
000020486 7001_ $$0P:(DE-HGF)0$$aGawronski, A.$$b1
000020486 7001_ $$0P:(DE-HGF)0$$aVolpert, K.$$b2
000020486 7001_ $$0P:(DE-HGF)0$$aSchilbach, L.$$b3
000020486 7001_ $$0P:(DE-HGF)0$$aTepest, R.$$b4
000020486 7001_ $$0P:(DE-HGF)0$$aHuff, W.$$b5
000020486 7001_ $$0P:(DE-Juel1)VDB1715$$aVogeley, K.$$b6$$uFZJ
000020486 773__ $$0PERI:(DE-600)2037701-0$$a10.1055/s-0031-1281642$$gVol. 80, p. 88 - 97$$p88 - 97$$q80<88 - 97$$tFortschritte der Neurologie, Psychiatrie$$v80$$x0720-4299$$y2012
000020486 8567_ $$uhttp://dx.doi.org/10.1055/s-0031-1281642
000020486 909CO $$ooai:juser.fz-juelich.de:20486$$pVDB
000020486 9132_ $$0G:(DE-HGF)POF3-572$$1G:(DE-HGF)POF3-570$$2G:(DE-HGF)POF3-500$$aDE-HGF$$bKey Technologies$$lDecoding the Human Brain$$v(Dys-)function and Plasticity$$x0
000020486 9131_ $$0G:(DE-HGF)POF2-89572$$1G:(DE-HGF)POF3-890$$2G:(DE-HGF)POF3-800$$3G:(DE-HGF)POF3$$4G:(DE-HGF)POF$$aDE-HGF$$bProgrammungebundene Forschung$$lohne Programm$$v(Dys-)function and Plasticity$$x1
000020486 9141_ $$y2012
000020486 915__ $$0StatID:(DE-HGF)0010$$2StatID$$aJCR/ISI refereed
000020486 915__ $$0StatID:(DE-HGF)0100$$2StatID$$aJCR
000020486 915__ $$0StatID:(DE-HGF)0110$$2StatID$$aWoS$$bScience Citation Index
000020486 915__ $$0StatID:(DE-HGF)0111$$2StatID$$aWoS$$bScience Citation Index Expanded
000020486 915__ $$0StatID:(DE-HGF)0150$$2StatID$$aDBCoverage$$bWeb of Science Core Collection
000020486 915__ $$0StatID:(DE-HGF)0199$$2StatID$$aDBCoverage$$bThomson Reuters Master Journal List
000020486 915__ $$0StatID:(DE-HGF)0200$$2StatID$$aDBCoverage$$bSCOPUS
000020486 915__ $$0StatID:(DE-HGF)0300$$2StatID$$aDBCoverage$$bMedline
000020486 915__ $$0StatID:(DE-HGF)0420$$2StatID$$aNationallizenz
000020486 915__ $$0StatID:(DE-HGF)1050$$2StatID$$aDBCoverage$$bBIOSIS Previews
000020486 915__ $$0StatID:(DE-HGF)1110$$2StatID$$aDBCoverage$$bCurrent Contents - Clinical Medicine
000020486 9201_ $$0I:(DE-Juel1)INM-3-20090406$$gINM$$kINM-3$$lKognitive Neurowissenschaften$$x0
000020486 970__ $$aVDB:(DE-Juel1)136034
000020486 980__ $$aVDB
000020486 980__ $$aConvertedRecord
000020486 980__ $$ajournal
000020486 980__ $$aI:(DE-Juel1)INM-3-20090406
000020486 980__ $$aUNRESTRICTED