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Ugeskr Laeger ; 184(34)2022 08 22.
Article in Danish | MEDLINE | ID: mdl-36065862

ABSTRACT

Autism spectrum disorders (ASD) have a complex genetic component comprising both frequent polygenic and rare monogenic factors. Research is conducted in methods used to calculate polygenic risk scores, which are not applicable in clinical practice. Advances in genomic technology have identified several monogenic causes, and genetic testing may be offered to persons with ASD where a monogenic etiology is suspected. Herein, we provide an overview of the current knowledge and present the first national recommendation regarding genetic testing in ASD.


Subject(s)
Autism Spectrum Disorder , Autism Spectrum Disorder/diagnosis , Autism Spectrum Disorder/genetics , Genetic Predisposition to Disease , Genetic Testing , Genomics , Humans
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