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dc.contributor.authorSkjeldal, Ola H
dc.contributor.authorIsaksen, Jørn
dc.date.accessioned2024-03-01T12:07:06Z
dc.date.available2024-03-01T12:07:06Z
dc.date.created2023-09-04T09:04:32Z
dc.date.issued2023
dc.identifier.citationTranslational Science of Rare Diseases. 2023, 6 (4), 101-115.en_US
dc.identifier.issn2214-6490
dc.identifier.urihttps://hdl.handle.net/11250/3120661
dc.description.abstractAutism is a group of neurodevelopmental disorders that involve definite impairments in social interactions, disturbance in language, and a stereotyped pattern of behaviour. These clinical features are described as the core symptoms. The condition represents a very large number of diseases and syndromes that are individually rare. Therefore, most people will refer to autism in the plural – autisms. The prevalence of autism has increased incredibly in the last three decades. However, although the number of people diagnosed with autism has increased, this is not the same as saying that there is an increase in the number of cases of autism. Most likely, many children and adults 40–50 years ago had autistic behaviour that went under other diagnoses. The cause of the autistic features has been thoroughly discussed for many years and has been the subject of many research activities. The dominant view today is that genetic and environmental factors mainly cause autism. In this article we want to give a brief status quo of the clinic, epidemiology and causes of autism.en_US
dc.description.abstractAutism – A brief updateen_US
dc.language.isoengen_US
dc.publisherIOS Pressen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.subjectAutismen_US
dc.subjectepidemiologyen_US
dc.subjectneurodevelopmental disordersen_US
dc.titleAutism – A brief updateen_US
dc.title.alternativeAutism – A brief updateen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holder© 2023 – The authors. Published by IOS Press. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (CC BY-NC 4.0).en_US
dc.source.pagenumber101-115en_US
dc.source.volume6en_US
dc.source.journalTranslational Science of Rare Diseasesen_US
dc.source.issue4en_US
dc.identifier.doi10.3233/TRD-230058
dc.identifier.cristin2171914
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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