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dc.contributor.authorAlaghband-Rad, Javad
dc.contributor.authorHamburger, Susan D.
dc.contributor.authorGiedd, Jay N.
dc.contributor.authorFrazier, Jean A.
dc.contributor.authorRapoport, Judith L.
dc.date2022-08-11T08:10:27.000
dc.date.accessioned2022-08-23T17:09:32Z
dc.date.available2022-08-23T17:09:32Z
dc.date.issued1997-01-01
dc.date.submitted2011-02-10
dc.identifier.citationAm J Psychiatry. 1997 Jan;154(1):64-8.
dc.identifier.issn0002-953X (Linking)
dc.identifier.pmid8988960
dc.identifier.urihttp://hdl.handle.net/20.500.14038/45844
dc.description.abstractOBJECTIVE: The purpose of this study was to examine the relationships between clinical and neurobiological measures of childhood-onset schizophrenia. It was hypothesized that there would be a more striking pattern in the rare cases with very early onset than is seen in subjects with later onset. METHOD: Premorbid, clinical, prenatal, perinatal, and magnetic resonance imaging brain measures were examined in 29 children and adolescents who met the DSM-III-R criteria for schizophrenia with onset before age 12. Specifically, gender, premorbid adjustment, and clinical symptoms were examined in relation to cerebral volume, ventricular volume, and maternal obstetrical complications. RESULTS: Males were more likely to have had an insidious onset than females. There was a significant negative correlation between score on the Scale for the Assessment of Negative Symptoms and total cerebral volume. CONCLUSIONS: These neurobiological associations support the continuity of early-onset schizophrenia with the later-onset disorder; the striking association between smaller cerebral volume and negative symptoms suggests a more homogeneous or more potent neurobiological basis for very early-onset schizophrenia.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=8988960&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://ajp.psychiatryonline.org/cgi/reprint/154/1/64
dc.subjectAdolescent
dc.subjectAge of Onset
dc.subjectBiological Markers
dc.subjectBrain
dc.subjectChild
dc.subjectChild Development Disorders, Pervasive
dc.subjectComorbidity
dc.subjectFemale
dc.subjectHumans
dc.subjectLanguage Disorders
dc.subjectMagnetic Resonance Imaging
dc.subjectPregnancy
dc.subjectPregnancy Complications
dc.subjectPsychiatric Status Rating Scales
dc.subjectSchizophrenia, Childhood
dc.subjectSex Factors
dc.subjectSocial Adjustment
dc.subjectPsychiatry
dc.titleChildhood-onset schizophrenia: biological markers in relation to clinical characteristics
dc.typeJournal Article
dc.source.journaltitleThe American journal of psychiatry
dc.source.volume154
dc.source.issue1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/psych_pp/373
dc.identifier.contextkey1775293
html.description.abstract<p>OBJECTIVE: The purpose of this study was to examine the relationships between clinical and neurobiological measures of childhood-onset schizophrenia. It was hypothesized that there would be a more striking pattern in the rare cases with very early onset than is seen in subjects with later onset.</p> <p>METHOD: Premorbid, clinical, prenatal, perinatal, and magnetic resonance imaging brain measures were examined in 29 children and adolescents who met the DSM-III-R criteria for schizophrenia with onset before age 12. Specifically, gender, premorbid adjustment, and clinical symptoms were examined in relation to cerebral volume, ventricular volume, and maternal obstetrical complications.</p> <p>RESULTS: Males were more likely to have had an insidious onset than females. There was a significant negative correlation between score on the Scale for the Assessment of Negative Symptoms and total cerebral volume.</p> <p>CONCLUSIONS: These neurobiological associations support the continuity of early-onset schizophrenia with the later-onset disorder; the striking association between smaller cerebral volume and negative symptoms suggests a more homogeneous or more potent neurobiological basis for very early-onset schizophrenia.</p>
dc.identifier.submissionpathpsych_pp/373
dc.contributor.departmentDepartment of Psychiatry
dc.source.pages64-8


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