| Subgroups in autism: are there behavioural phenotypes typical of underlying medical conditions? | |
| | |
MedLine Citation:
|
PMID: 1623312 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
|
Fifty-nine cases with infantile autism/autistic disorder were subclassified according to associated medical condition (fragile-X, tuberous sclerosis, neurofibromatosis, hypo-melanosis of Ito, Moebius syndrome, Rett syndrome, and a 'new' syndrome associated with a marker chromosome). It was concluded that, even within a group of cases fitting currently accepted criteria for autism, there is considerable variation in symptom profile depending on the exact type of associated medical condition. |
| | |
Authors:
|
C Gillberg |
Publication Detail:
|
Type: Journal Article; Research Support, Non-U.S. Gov't |
Journal Detail:
|
Title: Journal of intellectual disability research : JIDR Volume: 36 ( Pt 3) ISSN: 0964-2633 ISO Abbreviation: J Intellect Disabil Res Publication Date: 1992 Jun |
Date Detail:
|
Created Date: 1992-08-11 Completed Date: 1992-08-11 Revised Date: 2006-11-15 |
Medline Journal Info:
|
Nlm Unique ID: 9206090 Medline TA: J Intellect Disabil Res Country: ENGLAND |
Other Details:
|
Languages: eng Pagination: 201-14 Citation Subset: IM |
Affiliation:
|
Department of Pediatrics and Child Psychiatry, University of Göteborg, Sweden. |
Export Citation:
|
APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
|
Adolescent Adult Autistic Disorder / diagnosis, genetics*, psychology Brain Damage, Chronic / diagnosis, genetics*, psychology Child Child, Preschool Delirium, Dementia, Amnestic, Cognitive Disorders / diagnosis, genetics*, psychology Diseases in Twins / genetics Female Fragile X Syndrome / diagnosis, genetics, psychology Genetic Markers / genetics Humans Male Middle Aged Neurofibromatosis 2 / diagnosis, genetics, psychology Neuropsychological Tests Phenotype* Pigmentation Disorders / diagnosis, genetics, psychology Rett Syndrome / diagnosis, genetics, psychology Tuberous Sclerosis / diagnosis, genetics, psychology |
| Chemical | |
Reg. No./Substance:
|
0/Genetic Markers |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
Previous Document: Recent psychiatric classification systems and their significance for forensic psychiatry
Next Document: Properties of perception of laterally moving objects in persons with profound retardation.